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

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..

Clearance details

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

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