HOME CLINIC PREGNANCY TEST— 510(k) K883826

Substantially Equivalent

Vanguard Biomedical Corp.

FDA 510(k) clearance K883826 for HOME CLINIC PREGNANCY TEST, Substantially Equivalent on 1988-11-29. Applicant: Vanguard Biomedical Corp..

Clearance details

Applicant: Vanguard Biomedical Corp.
Product code: Code LCX
Advisory panel: Clinical Chemistry
Date received: 1988-09-09
Decision date: 1988-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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