Cleared Traditional

K926090 - SYVA MICROTRAK(R) II CHLAMYDIA EIA BLOCK REAGENT (FDA 510(k) Clearance)

Sep 1993
Decision
302d
Days
Class 1
Risk

K926090 is an FDA 510(k) clearance for the SYVA MICROTRAK(R) II CHLAMYDIA EIA BLOCK REAGENT. This device is classified as a Enzyme Linked Immunoabsorbent Assay, (chlamydiae Group) (Class I - General Controls, product code LJC).

Submitted by Syva Co. (San Jose, US). The FDA issued a Cleared decision on September 30, 1993, 302 days after receiving the submission on December 2, 1992.

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

Submission Details

510(k) Number K926090 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 02, 1992
Decision Date September 30, 1993
Days to Decision 302 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Summary PDF

Device Classification

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