Glu

FDA 510(k) K981185 · Abbott Laboratories

Substantially Equivalent

510(k) numberK981185

Submission

Device name
Glu
Applicant
Abbott Laboratories
Irving, TX, US
Received
April 2, 1998
Decision date
May 7, 1998
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

Other 510(k)s with product code CFR

510(k)DeviceApplicantDecision
K253490Glucose HK Gen.3; ONLINE DAT Methadone II; cobas pro integrated solutionsCFR · Traditional Roche Diagnostics02/12/2026SE
K252357Glucose2CFR · Traditional Abbott Ireland10/24/2025SE
K220134cobas pure integrated solutions, Glucose HK Gen.3, ISE indirect Na for Gen.2, ONLINE DAT…CFR · Traditional Roche Diagnostics09/16/2022SE
K191899Glucose HK Gen.3, ISE indirect Na for Gen.2, Elecsys TSH, cobas pro integrated solutionsCFR · Traditional Roche Diagnostics08/16/2019SE
K170316Alinity C Glucose Reagent Kit, Alinity C SystemCFR · Traditional Abbott Laboratories10/19/2017SE
K153644ELITech Clinical Systems GLUCOSE HK SL, ELITech Clinical Systems ELICAL 2, ELITech…CFR · Traditional Elitechgroup09/07/2016SE
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
K123018Ace Alera Clinical Chemistry System, Ace Glucose Reagent, Ace Ion Selective Electrode…CFR · Traditional Alfa Wassermann Diagnostic Technologies, Inc.04/23/2013SE
K120681Advia Chemistry GLUH_3 ReagentsCFR · Traditional Siemens Healthcare Diagnostics, Inc.05/15/2012SE

More from Siemens Healthcare Diagnostics, Inc.

510(k)DeviceDecision
K252424Anti-HCV NextMZO · Traditional 04/28/2026SE
K243500ARCHITECT iGentamicinLCD · Special 07/09/2025SE
K243168Alinity i Rubella IgGLFX · Traditional 06/20/2025SE
K243283Alinity h-series SystemGKZ · Traditional 02/20/2025SE
K233932Alinity i Toxo IgMLGD · Traditional 08/30/2024SE
K232669TbiQAT · Special 09/29/2023SE
K222850HAVAb IgG IILOL · Traditional 08/10/2023SE
K220031Alinity h-series SystemGKZ · Traditional 08/04/2023SE
K220282i-STAT PTplus Cartridge with the i-STAT 1 SystemGJS · Traditional 07/14/2023SE
K230937Alinity i Total ß-hCG Reagent Kit, GLP systems TrackDHA · Traditional 06/05/2023SE

Questions and answers

When was Glu cleared by the FDA?

Glu (K981185) received a 510(k) decision of Substantially Equivalent on May 7, 1998, 35 days after the submission was received.

What is the product code of K981185?

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