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

Name: FDA 510(k) clearance K860498
Creator: U.S. Food and Drug Administration
Published: 1986-07-16

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.. Device class: 2.

Clearance details

Applicant: Gen-Probe, Inc.
Product code: Code LQH
Device class: Class 2
Regulation: 21 CFR 866.3300
Advisory panel: Microbiology
Date received: 1986-02-10
Decision date: 1986-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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