HOME PREGNANCY TEST KIT— 510(k) K831108

Substantially Equivalent

Quidel Corp.

FDA 510(k) clearance K831108 for HOME PREGNANCY TEST KIT, Substantially Equivalent on 1983-05-18. Applicant: Quidel Corp..

Clearance details

Applicant: Quidel Corp.
Product code: Code LCX
Advisory panel: Clinical Chemistry
Date received: 1983-04-05
Decision date: 1983-05-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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