Systemate Glucose 67216

FDA 510(k) K843150 · Em Diagnostic Systems, Inc.

Substantially Equivalent

510(k) numberK843150

Submission

Device name
Systemate Glucose 67216
Applicant
Em Diagnostic Systems, Inc.
Mchenry, IL, US
Received
August 10, 1984
Decision date
August 27, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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
K935181Aspartate Aminotransferase (Ast) TestCIT · Traditional 01/27/1994SE
K935180Alanine Aminotransferase (Alt) TestCKA · Traditional 01/13/1994SE
K935179Emds Albumin (Alb) TestCIX · Traditional 12/17/1993SE
K935178Emds Phosphorous (Phos) TestCEO · Traditional 12/17/1993SE
K935177Gamma-Glutamyl Transferase (GGT) TestJQB · Traditional 12/16/1993SE
K935176Iron TestJIY · Traditional 12/16/1993SE
K935175Lactate Dehydrogenase (LD)CFJ · Traditional 12/16/1993SE
K935174Total Protein Test (Tpro)CEK · Traditional 12/16/1993SE
K935136Cholesterol (Chol) Test Item No. 65410CHH · Traditional 12/16/1993SE
K935183Emds Magnesium (MG) TestJGJ · Traditional 12/09/1993SE

Questions and answers

When was Systemate Glucose 67216 cleared by the FDA?

Systemate Glucose 67216 (K843150) received a 510(k) decision of Substantially Equivalent on August 27, 1984, 17 days after the submission was received.

What is the product code of K843150?

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