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ABBOTT QLUICKSTART IRON TEST, ITEM #5A29

K913705 Class I Traditional
Decision Date
1991-10-09
Sponsor / Applicant
Em Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K913705
Product Code CFM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1410
Decision Date 1991-10-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABBOTT QLUICKSTART IRON TEST, ITEM #5A29 received FDA 510(k) clearance under submission number K913705, sponsored by Em Diagnostic Systems, 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 1991-10-09.

Classification & Regulation

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