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RIA KIT, FERRITIN SOLID PHASE

K781946 Class II Traditional
Decision Date
1979-01-10
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K781946
Product Code JMG
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5340
Decision Date 1979-01-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RIA KIT, FERRITIN SOLID PHASE received FDA 510(k) clearance under submission number K781946, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1979-01-10.

Classification & Regulation

This clearance is catalogued under FDA product code JMG and 21 CFR 866.5340, within the Immunology review panel as a Class II device.