Cleared Traditional

K981401 - BOEHRINGER MANNHEIM PRECINORM PRECIPATH PROTEIN CONTROLS (FDA 510(k) Clearance)

May 1998
Decision
31d
Days
Class 1
Risk

K981401 is an FDA 510(k) clearance for the BOEHRINGER MANNHEIM PRECINORM PRECIPATH PROTEIN CONTROLS. 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 May 18, 1998, 31 days after receiving the submission on April 17, 1998.

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

Submission Details

510(k) Number K981401 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 17, 1998
Decision Date May 18, 1998
Days to Decision 31 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

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