MINICLINIC OVULATION PREDICTION TEST— 510(k) K891762

Name: FDA 510(k) clearance K891762
Creator: U.S. Food and Drug Administration
Published: 1989-07-20

Substantially Equivalent

Vanguard Biomedical Corp.

FDA 510(k) clearance K891762 for MINICLINIC OVULATION PREDICTION TEST, Substantially Equivalent on 1989-07-20. Applicant: Vanguard Biomedical Corp.. Device class: 1.

Clearance details

Applicant: Vanguard Biomedical Corp.
Product code: Code CEP
Device class: Class 1
Regulation: 21 CFR 862.1485
Advisory panel: Clinical Chemistry
Date received: 1989-03-24
Decision date: 1989-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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