MINICLINIC OVULATION PREDICTION TEST— 510(k) K910351

Name: FDA 510(k) clearance K910351
Creator: U.S. Food and Drug Administration
Published: 1991-03-21

Substantially Equivalent

Vanguard Biomedical Corp.

FDA 510(k) clearance K910351 for MINICLINIC OVULATION PREDICTION TEST, Substantially Equivalent on 1991-03-21. 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: 1991-01-15
Decision date: 1991-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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