meddevicedb.com FDA Device Reference

KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT

K933329 Class I Traditional
Decision Date
1993-10-22
Sponsor / Applicant
King Diagnostics, Inc.

Technical Specification

510(k) Submission ID K933329
Product Code JMO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1415
Decision Date 1993-10-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT received FDA 510(k) clearance under submission number K933329, sponsored by King 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 1993-10-22.

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.