meddevicedb.com FDA Device Reference

NSULIN RIA KIT 125I

K771628 Class I Traditional
Decision Date
1977-09-20
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K771628
Product Code CFP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1405
Decision Date 1977-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NSULIN RIA KIT 125I received FDA 510(k) clearance under submission number K771628, 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 1977-09-20.

Classification & Regulation

This clearance is catalogued under FDA product code CFP and 21 CFR 862.1405, within the Clinical Chemistry review panel as a Class I device.