QUICK VUE RSV TEST, MODELS 20193, 20199— 510(k) K070747

Name: FDA 510(k) clearance K070747
Creator: U.S. Food and Drug Administration
Published: 2007-04-23

Substantially Equivalent

Quidel Corp.

FDA 510(k) clearance K070747 for QUICK VUE RSV TEST, MODELS 20193, 20199, Substantially Equivalent on 2007-04-23. Applicant: Quidel Corp.. Device class: 1.

Clearance details

Applicant: Quidel Corp.
Product code: Code GQG
Device class: Class 1
Regulation: 21 CFR 866.3480
Advisory panel: Microbiology
Date received: 2007-03-19
Decision date: 2007-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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