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SERUM IRON

K771838 Class I Traditional
Decision Date
1977-11-03
Sponsor / Applicant
Gamma Enterprises, Inc.

Technical Specification

510(k) Submission ID K771838
Product Code JIY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1410
Decision Date 1977-11-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SERUM IRON received FDA 510(k) clearance under submission number K771838, sponsored by Gamma Enterprises, 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 1977-11-03.

Classification & Regulation

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