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KODAK EKTACHEM CLINICAL CHEMISTRY SLIDES (PHOS)

K932729 Class I Traditional
Decision Date
1993-08-03
Sponsor / Applicant
Eastman Kodak Company

Technical Specification

510(k) Submission ID K932729
Product Code CEO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1580
Decision Date 1993-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KODAK EKTACHEM CLINICAL CHEMISTRY SLIDES (PHOS) received FDA 510(k) clearance under submission number K932729, sponsored by Eastman Kodak Company. 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 1993-08-03.

Classification & Regulation

This clearance is catalogued under FDA product code CEO and 21 CFR 862.1580, within the Clinical Chemistry review panel as a Class I device.