KODAK DIGITAL SCIENCE 9000D MEDICAL LASER PRINTER (9000D)— 510(k) K972847

Name: FDA 510(k) clearance K972847
Creator: U.S. Food and Drug Administration
Published: 1997-10-07

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K972847 for KODAK DIGITAL SCIENCE 9000D MEDICAL LASER PRINTER (9000D), Substantially Equivalent on 1997-10-07. Applicant: Eastman Kodak Company. Device class: 2.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 1997-08-01
Decision date: 1997-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

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