Cleared Traditional

K842521 - AST/GOT REAGENT SET UV RATE
(FDA 510(k) Clearance)

Aug 1984
Decision
46d
Days
Class 2
Risk

K842521 is an FDA 510(k) clearance for the AST/GOT REAGENT SET UV RATE. This device is classified as a Nadh Oxidation/nad Reduction, Ast/sgot (Class II - Special Controls, product code CIT).

Submitted by Sterling Biochemical, Inc. (Mchenry, US). The FDA issued a Cleared decision on August 12, 1984, 46 days after receiving the submission on June 27, 1984.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1100.

Submission Details

510(k) Number K842521 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 27, 1984
Decision Date August 12, 1984
Days to Decision 46 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code CIT — Nadh Oxidation/nad Reduction, Ast/sgot
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1100

Similar Devices — CIT Nadh Oxidation/nad Reduction, Ast/sgot

All 138
AST/GOT 4+1 SL, AST/GOT 4+1 SL, ELICAL 2, ELITROL I, ELITROL II, MODEL ASSL-0250, ASSL-0455, CALI-0580, CONT-0080, CONT-
K093883 · Seppim S.A.S. · Sep 2010
ASPARTATE AMINO TRANSFERASE (AST/SGOT) TEST SYSTEM, ASAT (GOT) FS
K080485 · Diasys Diagnostics Systems GmbH · Dec 2008
ACTIVATED ASPARTATE AMINOTRANSFERASE
K071525 · Abbott Laboratories · Mar 2008
AST/GOT (IFCC), PYRIDOXAL PHOSPHATE, ECAL, NORTROL AND ABTROL
K071580 · Thermofisher Scientific OY · Oct 2007
COBAS C 111 ANALYZER
K071211 · Roche Diagnostics · Jul 2007
HEPATIC ENZYMES ON ABX PENTRA 400 CLINICAL CHEMISTRY ANALYZER
K060318 · Horiba Abx · Aug 2006