GEN-PROBE MYCOPLASMA PNEUMONIA RAPID DETECT SYSTEM— 510(k) K860574

Substantially Equivalent

Gen-Probe, Inc.

FDA 510(k) clearance K860574 for GEN-PROBE MYCOPLASMA PNEUMONIA RAPID DETECT SYSTEM, Substantially Equivalent on 1986-07-03. Applicant: Gen-Probe, Inc..

Clearance details

Applicant: Gen-Probe, Inc.
Product code: Code LQG
Advisory panel: Microbiology
Date received: 1986-02-14
Decision date: 1986-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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