The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
May. 30, 2023

Filed:

Mar. 31, 2022
Applicant:

Magnolia Medical Technologies, Inc., Seattle, WA (US);

Inventors:

Gregory J. Bullington, Seattle, WA (US);

Richard G. Patton, Seattle, WA (US);

Shan E. Gaw, Seattle, WA (US);

Assignee:
Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61B 5/15 (2006.01); A61B 5/153 (2006.01); A61B 10/00 (2006.01); A61B 5/154 (2006.01); A61B 5/155 (2006.01); B01L 3/02 (2006.01);
U.S. Cl.
CPC ...
A61B 5/150251 (2013.01); A61B 5/1405 (2013.01); A61B 5/1416 (2013.01); A61B 5/1427 (2013.01); A61B 5/1438 (2013.01); A61B 5/15003 (2013.01); A61B 5/153 (2013.01); A61B 5/154 (2013.01); A61B 5/155 (2013.01); A61B 5/150221 (2013.01); A61B 5/150236 (2013.01); A61B 5/150244 (2013.01); A61B 5/150343 (2013.01); A61B 5/150389 (2013.01); A61B 5/150633 (2013.01); A61B 10/0045 (2013.01); A61B 5/150732 (2013.01); B01L 3/0231 (2013.01);
Abstract

A syringe-based device includes a housing, a pre-sample reservoir, and an actuator. The housing defines an inner volume between a substantially open proximal end portion and a distal end portion that includes a port couplable to a lumen-defining device. The pre-sample reservoir is fluidically couplable to the port to receive and isolate a first volume of bodily fluid. The actuator is at least partially disposed in the inner volume and has a proximal end portion that includes an engagement portion and a distal end portion that includes a sealing member. The engagement portion is configured to allow a user to selectively move the actuator between a first configuration such that bodily fluid can flow from the port to the pre-sample reservoir, and a second configuration such that bodily fluid can flow from the port to a sample reservoir defined at least in part by the sealing member and the housing.


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