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T4 NO SPIN(TM) COATED TUBE RADIOIMMUNOASSAY KIT

K870573 Class II Traditional
Decision Date
1987-04-22
Sponsor / Applicant
Cambridge Medical Technology

Technical Specification

510(k) Submission ID K870573
Product Code CDX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1700
Decision Date 1987-04-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

T4 NO SPIN(TM) COATED TUBE RADIOIMMUNOASSAY KIT received FDA 510(k) clearance under submission number K870573, sponsored by Cambridge Medical Technology. 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 1987-04-22.

Classification & Regulation

This clearance is catalogued under FDA product code CDX and 21 CFR 862.1700, within the Clinical Chemistry review panel as a Class II device.