MONOFLUOR CHLAMYDIA TRACHOMATIS DIR SPEC TEST KIT— 510(k) K862354

Name: FDA 510(k) clearance K862354
Creator: U.S. Food and Drug Administration
Published: 1986-09-29

Substantially Equivalent

Synbiotics Corp.

FDA 510(k) clearance K862354 for MONOFLUOR CHLAMYDIA TRACHOMATIS DIR SPEC TEST KIT, Substantially Equivalent on 1986-09-29. Applicant: Synbiotics Corp.. Device class: 1.

Clearance details

Applicant: Synbiotics Corp.
Product code: Code LJP
Device class: Class 1
Regulation: 21 CFR 866.3120
Advisory panel: Microbiology
Date received: 1986-06-20
Decision date: 1986-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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