Cleared Traditional

K954894 - HYTEC AUTOIMMUNE KITS (SCL-70)
(FDA 510(k) Clearance)

Mar 1996
Decision
183d
Days
Class 2
Risk

K954894 is an FDA 510(k) clearance for the HYTEC AUTOIMMUNE KITS (SCL-70). This device is classified as a Extractable Antinuclear Antibody, Antigen And Control (Class II - Special Controls, product code LLL).

Submitted by Hycor Biomedical, Inc. (Garden Grove, US). The FDA issued a Cleared decision on March 20, 1996, 183 days after receiving the submission on September 19, 1995.

This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5100.

Submission Details

510(k) Number K954894 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 19, 1995
Decision Date March 20, 1996
Days to Decision 183 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary Statement

Device Classification

Product Code LLL — Extractable Antinuclear Antibody, Antigen And Control
Device Class Class II - Special Controls
CFR Regulation 21 CFR 866.5100

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