Abbott Diabetes Care Inc.

Intuity Medical, Inc.

Therasense, Inc.

Lifescan Corporation

E. Heller & Company

Pepex Biomedical, L.l.c.

Michael F Tomasco

James L Say

Adam Heller

Phillip John Plante

Yoram Gal

Ephraim Heller

Mark S Vreeke

Behrad Aria

Fredric C Colman

Keith A Friedman

Raul Escutia

Paul D Reynolds

Kelley J Lipman

John Frederick Larkin

Charles Hu

Jeffrey L Emery

Edward G Rice

Joseph A Vivolo

Daniel Ray Bloom

Ernest J Kiser

Robin S Gaffney

Christopher L Stewart

Kimberly J Tansey

Peter Uy-Vu Ly

Aria Behrad

Robert W Bowers

Craig M Litherland

Richard M Wiard

David K Hohl

Jeffrey M Jones

Raúl Escutia

Daniel Nicholas Brncic

Henning Sakslund

Jennifer Y Blomo

Hyun Brian Cho

Jay Douglas Audett

Duane O Yamasaki

Remedios Dato

Joel Sterling Douglas

Gregory Loney

Yeung Siu Yu

Maria Teodorczyk

Scott Segelke

Deborah P Tuohy

Jennifer Yuh-Jen Chen

Mark Maxson

Zbigniew Witko

Joe Vivolo

Cheung Peng Hu

A medical diagnostic device includes a wirelessly transmitted time data receiver and processor. Associated devices, methods and functionality are also described.

Medical diagnostic devices and methods

A device includes: a first portion configured to be grasped by the hand of the user, and a second portion defining a reservoir containing a control material, wherein the control material contains a target analyte in a known or predetermined concentration. A method of verifying the accuracy of an analyte monitoring device includes receiving a fluid sample, identifying the fluid sample as a control solution, and analyzing the fluid sample.

Calibration material delivery devices and methods

Described here are meters and methods for sampling, transporting, and/or analyzing a fluid sample. The meters may include a meter housing and a cartridge. In some instances, the meter may include a tower which may engage one or more portions of a cartridge. The meter housing may include an imaging system, which may or may not be included in the tower. The cartridge may include one or more sampling arrangements, which may be configured to collect a fluid sample from a sampling site. A sampling arrangement may include a skin-penetration member, a hub, and a quantification member.

Devices and methods for body fluid sampling and analysis

A method for performing an assay to determine the presence or concentration of an analyte contained in a sample of body fluid by using a device comprising at least one analyte quantification member and a sensor associated therewith, the method includes: applying a first sample to the analyte quantification member; and detecting the presence or absence of an adequate sample volume; wherein upon detection of the absence of an adequate sample volume, initiating a finite timed period, and signaling the user to introduce a second sample of body fluid to the analyte quantification member. Associated arrangements and devices are also disclosed.

Detection meter and mode of operation

An arrangement for producing a sample of body fluid from a wound opening created in a skin surface at a sampling site includes: a housing, the housing comprising a first opening; a skin interface member disposed in the first opening, the skin interface member comprising an inner member having a second opening, and an outer member at least partially surrounding the inner member and attached to the first opening; and at least one skin-penetration member configured and arranged to project within the second opening. Arrangements having alternatively constructed skin interface members are also described.

Body fluid sampling device-sampling site interface

A device includes: a first portion configured to be grasped by the hand of the user, and a second portion defining a reservoir containing a control material, wherein the control material contains a target analyte in a known or predetermined concentration. A method of verifying the accuracy of an analyte monitoring device includes receiving control information, receiving a fluid sample, identifying the fluid sample as a control solution, and analyzing the control solution.

A device includes: a first portion configured to be grasped by the hand of the user, and a second portion defining a reservoir containing a control material, wherein the control material contains a target analyte in a known or predetermined concentration. Methods for verifying the accuracy of an analyte monitoring device include receiving control information from a test cartridge, transporting control material to an analysis site, determining the presence of the control material, analyzing the control material, and providing a pass or fail signal.

Body fluid sampling device&#x2014;sampling site interface

An analyte monitor includes a sensor, a sensor control unit, and a display unit. The sensor has, for example, a substrate, a recessed channel formed in the substrate, and conductive material disposed in the recessed channel to form a working electrode. The sensor control unit typically has a housing adapted for placement on skin and is adapted to receive a portion of an electrochemical sensor. The sensor control unit also includes two or more conductive contacts disposed on the housing and configured for coupling to two or more contact pads on the sensor. A transmitter is disposed in the housing and coupled to the plurality of conductive contacts for transmitting data obtained using the sensor. The display unit has a receiver for receiving data transmitted by the transmitter of the sensor control unit and a display coupled to the receiver for displaying an indication of a level of an analyte. The analyte monitor may also be part of a drug delivery system to alter the level of the analyte based on the data obtained using the sensor.

Analyte monitoring device and methods of use

Growing community of inventors

Cupertino, CA, United States of America

Michael F Tomasco