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UPTAKE T3 RADIOIMMUNOASSAY KIT

K830900 Class II Traditional
Decision Date
1983-04-18
Sponsor / Applicant
Medical & Scientific Designs, Inc.

Technical Specification

510(k) Submission ID K830900
Product Code KHQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1715
Decision Date 1983-04-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UPTAKE T3 RADIOIMMUNOASSAY KIT received FDA 510(k) clearance under submission number K830900, sponsored by Medical & Scientific Designs, 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 1983-04-18.

Classification & Regulation

This clearance is catalogued under FDA product code KHQ and 21 CFR 862.1715, within the Clinical Chemistry review panel as a Class II device.