KODAK DIGITAL SCIENCES (KDS) IMAGE VIEW— 510(k) K981053

Name: FDA 510(k) clearance K981053
Creator: U.S. Food and Drug Administration
Published: 1998-06-18

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K981053 for KODAK DIGITAL SCIENCES (KDS) IMAGE VIEW, Substantially Equivalent on 1998-06-18. Applicant: Eastman Kodak Company. Device class: 1.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1998-03-23
Decision date: 1998-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

Download summary PDF View on FDA.gov ↗

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