Cleared Traditional

K040277 - LIQUICHEK CARDIAC MARKER CONTROL LT (FDA 510(k) Clearance)

Mar 2004
Decision
34d
Days
Class 1
Risk

K040277 is an FDA 510(k) clearance for the LIQUICHEK CARDIAC MARKER CONTROL LT. This device is classified as a Multi-analyte Controls, All Kinds (assayed) (Class I - General Controls, product code JJY).

Submitted by Bio-Rad Laboratories, Inc. (Irvine, US). The FDA issued a Cleared decision on March 10, 2004, 34 days after receiving the submission on February 5, 2004.

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

Submission Details

510(k) Number K040277 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 05, 2004
Decision Date March 10, 2004
Days to Decision 34 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