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MINICLINIC OVULATION PREDICTOR

K960233 Class I Traditional
Decision Date
1996-04-23
Sponsor / Applicant
Vanguard Biomedical Corp.

Technical Specification

510(k) Submission ID K960233
Product Code CEP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1485
Decision Date 1996-04-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MINICLINIC OVULATION PREDICTOR received FDA 510(k) clearance under submission number K960233, 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 1996-04-23.

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.