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IRON/UIBC REAGENT

K932517 Class I Traditional
Decision Date
1993-11-09
Sponsor / Applicant
Sigma Diagnostics, Inc.

Technical Specification

510(k) Submission ID K932517
Product Code JMO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1415
Decision Date 1993-11-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IRON/UIBC REAGENT received FDA 510(k) clearance under submission number K932517, sponsored by Sigma Diagnostics, 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 1993-11-09.

Classification & Regulation

This clearance is catalogued under FDA product code JMO and 21 CFR 862.1415, within the Clinical Chemistry review panel as a Class I device.