LH GEN III SELF-TEST/CONCEIVE— 510(k) K920160

Substantially Equivalent

Quidel Corp.

FDA 510(k) clearance K920160 for LH GEN III SELF-TEST/CONCEIVE, Substantially Equivalent on 1992-03-11. Applicant: Quidel Corp.. Device class: 1.

Clearance details

Applicant: Quidel Corp.
Product code: Code CEP
Device class: Class 1
Regulation: 21 CFR 862.1485
Advisory panel: Clinical Chemistry
Date received: 1992-01-14
Decision date: 1992-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.