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MINICLINIC OVULATION PREDICTION TEST

K891762 Class I Traditional
Decision Date
1989-07-20
Sponsor / Applicant
Vanguard Biomedical Corp.

Technical Specification

510(k) Submission ID K891762
Product Code CEP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1485
Decision Date 1989-07-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MINICLINIC OVULATION PREDICTION TEST received FDA 510(k) clearance under submission number K891762, sponsored by Vanguard Biomedical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1989-07-20.

Classification & Regulation

This clearance is catalogued under FDA product code CEP and 21 CFR 862.1485, within the Clinical Chemistry review panel as a Class I device.