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QTEST PREGNANCY TEST CONTROL

K883741 Class I Traditional
Decision Date
1988-10-03
Sponsor / Applicant
Quidel Corp.

Technical Specification

510(k) Submission ID K883741
Product Code JJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1988-10-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QTEST PREGNANCY TEST CONTROL received FDA 510(k) clearance under submission number K883741, sponsored by Quidel 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 1988-10-03.

Classification & Regulation

This clearance is catalogued under FDA product code JJX and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.