Cleared Traditional

K990624 - AUTOSTAT II ANTI-SM/RNP ELISA
(FDA 510(k) Clearance)

K990624 · Cogent Diagnotics , Ltd. · Immunology
Apr 1999
Decision
62d
Days
Class 2
Risk

K990624 is an FDA 510(k) clearance for the AUTOSTAT II ANTI-SM/RNP ELISA, a Anti-rnp Antibody, Antigen And Control (Class II — Special Controls, product code LKO), submitted by Cogent Diagnotics , Ltd. (Midlothian, Scotland, GB). The FDA issued a Cleared decision on April 28, 1999, 62 days after receiving the submission on February 25, 1999. This device falls under the Immunology review panel. Regulated under 21 CFR 866.5100.

Submission Details

510(k) Number K990624 FDA.gov
FDA Decision Cleared SESE
Date Received February 25, 1999
Decision Date April 28, 1999
Days to Decision 62 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary Statement

Device Classification

Product Code LKO — Anti-rnp Antibody, Antigen And Control
Device Class Class II — Special Controls
CFR Regulation 21 CFR 866.5100

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