Cleared Traditional

K902536 - PRECINORM(R) IM NORMAL IMMUNOASSAY CONTROL SERUM (FDA 510(k) Clearance)

Jul 1990
Decision
33d
Days
Class 1
Risk

K902536 is an FDA 510(k) clearance for the PRECINORM(R) IM NORMAL IMMUNOASSAY CONTROL SERUM. This device is classified as a Multi-analyte Controls, All Kinds (assayed) (Class I - General Controls, product code JJY).

Submitted by Boehringer Mannheim Corp. (Indianapolis, US). The FDA issued a Cleared decision on July 10, 1990, 33 days after receiving the submission on June 7, 1990.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1660.

Submission Details

510(k) Number K902536 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 07, 1990
Decision Date July 10, 1990
Days to Decision 33 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code JJY — Multi-analyte Controls, All Kinds (assayed)
Device Class Class I - General Controls
CFR Regulation 21 CFR 862.1660