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SIMUL-FER SERUM IRON TEST KIT

K820253 Class I Traditional
Decision Date
1982-05-12
Sponsor / Applicant
Diagnostic Reagents, Inc.

Technical Specification

510(k) Submission ID K820253
Product Code JJA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1410
Decision Date 1982-05-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIMUL-FER SERUM IRON TEST KIT received FDA 510(k) clearance under submission number K820253, sponsored by Diagnostic Reagents, 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 1982-05-12.

Classification & Regulation

This clearance is catalogued under FDA product code JJA and 21 CFR 862.1410, within the Clinical Chemistry review panel as a Class I device.