Systemate Got 67208

FDA 510(k) K843333 · Em Diagnostic Systems, Inc.

Substantially Equivalent

510(k) numberK843333

Submission

Device name
Systemate Got 67208
Applicant
Em Diagnostic Systems, Inc.
Mchenry, IL, US
Received
August 27, 1984
Decision date
September 20, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CIT – Nadh Oxidation/Nad Reduction, Ast/Sgot
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1100
Specialty
Clinical Chemistry

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K071525Activated Aspartate AminotransferaseCIT · Traditional Abbott Laboratories03/19/2008SE
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K071211Cobas C 111 AnalyzerCIT · Traditional Roche Diagnostics07/30/2007SE
K060318Hepatic Enzymes on Abx Pentra 400 Clinical Chemistry AnalyzerCIT · Traditional Horiba Abx08/08/2006SE
K023551Wiener Lab Got (Ast) UV Aa LiquidaCIT · Traditional Wiener Laboratories Saic12/09/2002SE
K013698Ast (Sgot)CIT · Traditional Jas Diagnostics, Inc.12/21/2001SE
K013145Wiener Lab. Got (Ast) UV Aa. Weiner Lab. Got (Ast) UV Unitest, Models 10 * 20 ML Cat.…CIT · Traditional Wiener Laboratories Saic11/27/2001SE
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More from Elan Holdings, 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 Got 67208 cleared by the FDA?

Systemate Got 67208 (K843333) received a 510(k) decision of Substantially Equivalent on September 20, 1984, 24 days after the submission was received.

What is the product code of K843333?

The FDA product code is CIT – Nadh Oxidation/Nad Reduction, Ast/Sgot, a Class II (moderate risk) device regulated under 21 CFR 862.1100.