KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM— 510(k) K060079

Name: FDA 510(k) clearance K060079
Creator: U.S. Food and Drug Administration
Published: 2006-02-08

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K060079 for KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM, Substantially Equivalent on 2006-02-08. Applicant: Eastman Kodak Company. Device class: 2.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code MUH
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2006-01-10
Decision date: 2006-02-08
Decision: Substantially Equivalent
Clearance type: Special
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

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