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:
Mar. 31, 2020

Filed:

May. 10, 2016
Applicant:

Exacsys Limited, London, GB;

Inventors:

Michael Noble, Melbourn, GB;

Craig Nelson, Melbourn, GB;

Mark Humphries, Melbourn, GB;

Carys Lloyd, Melbourn, GB;

David Edington, Melbourn, GB;

John Rippeth, Melbourn, GB;

Assignee:

PA Knowledge Limited, London, GB;

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
G01N 27/327 (2006.01); G01N 33/49 (2006.01); C12Q 1/00 (2006.01); C12Q 1/54 (2006.01);
U.S. Cl.
CPC ...
G01N 27/3272 (2013.01); C12Q 1/006 (2013.01); C12Q 1/54 (2013.01); G01N 27/3271 (2013.01); G01N 27/3274 (2013.01); G01N 33/4915 (2013.01); G01N 33/49 (2013.01); G01N 2496/00 (2013.01);
Abstract

A method and device are provided for measuring a level of a clinically relevant analyte (such as glucose) in a fluid (such as blood). The device includes a flow path for conducting said fluid through the device; a detection chamber arranged on said flow path; and detector means arranged to detect analyte levels in the fluid in said chamber, wherein: said detection chamber contains a predetermined amount of an analyte such that that analyte mixes with fluid in the detection chamber to form, at the detector means, a calibration sample of the fluid at a time after the arrival of the fluid in said detection chamber, and said detector means is arranged to detect a first analyte level of an unadulterated sample of the fluid at a first time which is before the formation of said calibration sample and to detect a second analyte level of said calibration sample at a second time which is after the formation of said calibration sample.


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