Cleared Traditional

K973196 - ZEUS SCIENTIFIC, INC., ANTI-CARDIOLIPIN IGA ELISA REAGENTS (FDA 510(k) Clearance)

Oct 1997
Decision
64d
Days
Class 2
Risk

K973196 is an FDA 510(k) clearance for the ZEUS SCIENTIFIC, INC., ANTI-CARDIOLIPIN IGA ELISA REAGENTS. This device is classified as a System, Test, Anticardiolipin Immunological (Class II - Special Controls, product code MID).

Submitted by Zeus Scientific, Inc. (Branchburg, US). The FDA issued a Cleared decision on October 29, 1997, 64 days after receiving the submission on August 26, 1997.

This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5660.

Submission Details

510(k) Number K973196 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 26, 1997
Decision Date October 29, 1997
Days to Decision 64 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary Statement

Device Classification

Product Code MID — System, Test, Anticardiolipin Immunological
Device Class Class II - Special Controls
CFR Regulation 21 CFR 866.5660