KODAK DIGITAL SCIENCE - DENTAL SCANNING SYSTEM— 510(k) K971894

Name: FDA 510(k) clearance K971894
Creator: U.S. Food and Drug Administration
Published: 1997-08-20

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K971894 for KODAK DIGITAL SCIENCE - DENTAL SCANNING SYSTEM, Substantially Equivalent on 1997-08-20. Applicant: Eastman Kodak Company. Device class: 2.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code LMA
Device class: Class 2
Regulation: 21 CFR 892.2030
Advisory panel: Radiology
Date received: 1997-05-22
Decision date: 1997-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.