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KIT, RIA, HUMAN THYROID HORMONE

K760044 Class II Traditional
Decision Date
1976-07-26
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K760044
Product Code JLW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1690
Decision Date 1976-07-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KIT, RIA, HUMAN THYROID HORMONE received FDA 510(k) clearance under submission number K760044, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. 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 1976-07-26.

Classification & Regulation

This clearance is catalogued under FDA product code JLW and 21 CFR 862.1690, within the Clinical Chemistry review panel as a Class II device.