Cleared Traditional

K955868 - BOEHRINGER MANNHEIM CARDIAC T TROPNIN T (FDA 510(k) Clearance)

Feb 1996
Decision
48d
Days
Class 2
Risk

K955868 is an FDA 510(k) clearance for the BOEHRINGER MANNHEIM CARDIAC T TROPNIN T. This device is classified as a Immunoassay Method, Troponin Subunit (Class II - Special Controls, product code MMI).

Submitted by Boehringer Mannheim Corp. (Indianapolis, US). The FDA issued a Cleared decision on February 14, 1996, 48 days after receiving the submission on December 28, 1995.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1215.

Submission Details

510(k) Number K955868 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 28, 1995
Decision Date February 14, 1996
Days to Decision 48 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

Product Code MMI — Immunoassay Method, Troponin Subunit
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1215

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