AMERLITE PROCESSING CENTER— 510(k) K915680

Name: FDA 510(k) clearance K915680
Creator: U.S. Food and Drug Administration
Published: 1992-03-11

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K915680 for AMERLITE PROCESSING CENTER, Substantially Equivalent on 1992-03-11. Applicant: Eastman Kodak Company. Device class: 1.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code JJQ
Device class: Class 1
Regulation: 21 CFR 862.2300
Advisory panel: Clinical Chemistry
Date received: 1991-12-19
Decision date: 1992-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

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