Glucose HK Gen.3; ONLINE DAT Methadone II; cobas pro integrated solutions

FDA 510(k) K253490 · Roche Diagnostics

Substantially Equivalent

510(k) numberK253490

Submission

Device name
Glucose HK Gen.3; ONLINE DAT Methadone II; cobas pro integrated solutions
Applicant
Roche Diagnostics
Indianapolis, IN, US
Received
October 24, 2025
Decision date
February 12, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CFR – Hexokinase, Glucose
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1345
Specialty
Clinical Chemistry

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K151487Diatron Pictus 700 Clinical Chemistry Analyzer, Diatron ISE, Diatron Glucose Hexokinase…CFR · Traditional Diatron U.S., Inc.01/14/2016SE
K131189Unicel DXC Synchron Systems Glucose Reagent (Gluh)CFR · Traditional Beckman Coulter, Inc.04/17/2014SE
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K120681Advia Chemistry GLUH_3 ReagentsCFR · Traditional Siemens Healthcare Diagnostics, Inc.05/15/2012SE
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Questions and answers

When was Glucose HK Gen.3; ONLINE DAT Methadone II; cobas pro integrated solutions cleared by the FDA?

Glucose HK Gen.3; ONLINE DAT Methadone II; cobas pro integrated solutions (K253490) received a 510(k) decision of Substantially Equivalent on February 12, 2026, 111 days after the submission was received.

What is the product code of K253490?

The FDA product code is CFR – Hexokinase, Glucose, a Class II (moderate risk) device regulated under 21 CFR 862.1345.