KODAK EKTACHEM DT SLIDES (FE)— 510(k) K934358

Name: FDA 510(k) clearance K934358
Creator: U.S. Food and Drug Administration
Published: 1994-03-21

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K934358 for KODAK EKTACHEM DT SLIDES (FE), Substantially Equivalent on 1994-03-21. Applicant: Eastman Kodak Company. Device class: 1.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code JQE
Device class: Class 1
Regulation: 21 CFR 862.1415
Advisory panel: Clinical Chemistry
Date received: 1993-09-08
Decision date: 1994-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

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