KODAK DIGITAL SCIENCE-DENTAL IMAGE VIEWER— 510(k) K973476

Name: FDA 510(k) clearance K973476
Creator: U.S. Food and Drug Administration
Published: 1997-11-10

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K973476 for KODAK DIGITAL SCIENCE-DENTAL IMAGE VIEWER, Substantially Equivalent on 1997-11-10. Applicant: Eastman Kodak Company. Device class: 2.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code EHD
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 1997-09-15
Decision date: 1997-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

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