GEN-PROBE LEGIONELLA RAPID DIAGNOSTIC SYSTEM— 510(k) K860498

Substantially Equivalent

Gen-Probe, Inc.

FDA 510(k) clearance K860498 for GEN-PROBE LEGIONELLA RAPID DIAGNOSTIC SYSTEM, Substantially Equivalent on 1986-07-16. Applicant: Gen-Probe, Inc..

Clearance details

Applicant: Gen-Probe, Inc.
Product code: Code LQH
Advisory panel: Microbiology
Date received: 1986-02-10
Decision date: 1986-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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