Cleared Traditional

TOTAL PROTEIN REAGENT KIT FOR ASTRA SYSTEMS

K884225 · A-Kem, Inc. · Chemistry
Dec 1988
Decision
64d
Days
Class 2
Risk

About This 510(k) Submission

K884225 is an FDA 510(k) clearance for the TOTAL PROTEIN REAGENT KIT FOR ASTRA SYSTEMS, a Biuret (colorimetric), Total Protein (Class II — Special Controls, product code CEK), submitted by A-Kem, Inc. (Clifton, US). The FDA issued a Cleared decision on December 9, 1988, 64 days after receiving the submission on October 6, 1988. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1635.

Submission Details

510(k) Number K884225 FDA.gov
FDA Decision Cleared SESE
Date Received October 06, 1988
Decision Date December 09, 1988
Days to Decision 64 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code CEK — Biuret (colorimetric), Total Protein
Device Class Class II — Special Controls
CFR Regulation 21 CFR 862.1635

Similar Devices — CEK Biuret (colorimetric), Total Protein

All 115
HICHEM TOTAL PROTEIN REAGENT
K992846 · Elan Holdings, Inc. · Oct 1999
TOTAL PROTEIN (MICRO) ASSAY, CATALOGUE NUMBER 450-50
K973108 · Diagnostic Chemicals , Ltd. · Mar 1998
CARESIDE TOTAL PROTEIN
K980042 · Exigent Diagnostics, Inc. · Feb 1998
TOTAL PROTEIN OR TP
K971524 · Carolina Liquid Chemistries Corp. · May 1997
CSF/URINE TOTAL PROTEIN
K961864 · Teco Diagnostics · Oct 1996
STC DIAGNOSTICS AUTO-LYTE URINARY PROTEIN ASSAY
K955905 · Solarcare Technologies Corp,Inc. · May 1996