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QUANTICOAT NEONATAL 125 T4 RADIOIMMUNO

K812611 Class II Traditional
Decision Date
1981-10-02
Sponsor / Applicant
Kallestad Laboratories, Inc.

Technical Specification

510(k) Submission ID K812611
Product Code CDP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1710
Decision Date 1981-10-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUANTICOAT NEONATAL 125 T4 RADIOIMMUNO received FDA 510(k) clearance under submission number K812611, sponsored by Kallestad Laboratories, 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 1981-10-02.

Classification & Regulation

This clearance is catalogued under FDA product code CDP and 21 CFR 862.1710, within the Clinical Chemistry review panel as a Class II device.