MINICLINIC OVULATION PREDICTOR— 510(k) K960233

Name: FDA 510(k) clearance K960233
Creator: U.S. Food and Drug Administration
Published: 1996-04-23

Substantially Equivalent

Vanguard Biomedical Corp.

FDA 510(k) clearance K960233 for MINICLINIC OVULATION PREDICTOR, Substantially Equivalent on 1996-04-23. 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: 1996-01-17
Decision date: 1996-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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