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COULTER SERUM IRON/UIBC REAGENT

K902173 Class I Traditional
Decision Date
1990-06-12
Sponsor / Applicant
Coulter Corp.

Technical Specification

510(k) Submission ID K902173
Product Code JIY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1410
Decision Date 1990-06-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COULTER SERUM IRON/UIBC REAGENT received FDA 510(k) clearance under submission number K902173, sponsored by Coulter Corp.. 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 1990-06-12.

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.