GEN-PROBE AMPLIFIED CHLAMYDIA TRACHOMATIS ASSAY KIT— 510(k) K962217

Name: FDA 510(k) clearance K962217
Creator: U.S. Food and Drug Administration
Published: 1996-11-27

Substantially Equivalent

Gen-Probe, Inc.

FDA 510(k) clearance K962217 for GEN-PROBE AMPLIFIED CHLAMYDIA TRACHOMATIS ASSAY KIT, Substantially Equivalent on 1996-11-27. Applicant: Gen-Probe, Inc.. Device class: 1.

Clearance details

Applicant: Gen-Probe, Inc.
Product code: Code MKZ
Device class: Class 1
Regulation: 21 CFR 866.3120
Advisory panel: Microbiology
Date received: 1996-06-10
Decision date: 1996-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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