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FIRST RESPONSE 10 MINUTE OVULATION PREDICTOR TEST

K883530 Class I Traditional
Decision Date
1988-12-19
Sponsor / Applicant
Tambrands, Inc.

Technical Specification

510(k) Submission ID K883530
Product Code CEP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1485
Decision Date 1988-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FIRST RESPONSE 10 MINUTE OVULATION PREDICTOR TEST received FDA 510(k) clearance under submission number K883530, sponsored by Tambrands, Inc.. 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 1988-12-19.

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.