Cleared Traditional

K903758 - SYVA MICROTRAK EIA ACCESSORY REAGENTS (FDA 510(k) Clearance)

Sep 1990
Decision
23d
Days
Class 1
Risk

K903758 is an FDA 510(k) clearance for the SYVA MICROTRAK EIA ACCESSORY REAGENTS. This device is classified as a Enzyme Linked Immunoabsorbent Assay, (chlamydiae Group) (Class I - General Controls, product code LJC).

Submitted by Syva Co. (Palo Alto, US). The FDA issued a Cleared decision on September 12, 1990, 23 days after receiving the submission on August 20, 1990.

This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.3120.

Submission Details

510(k) Number K903758 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 20, 1990
Decision Date September 12, 1990
Days to Decision 23 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary

Device Classification

Product Code LJC — Enzyme Linked Immunoabsorbent Assay, (chlamydiae Group)
Device Class Class I - General Controls
CFR Regulation 21 CFR 866.3120