KODAK EKTASCAN IMAGE TRANS. T1/R1 & P1 SOFTWARE— 510(k) K871984

Name: FDA 510(k) clearance K871984
Creator: U.S. Food and Drug Administration
Published: 1987-08-12

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K871984 for KODAK EKTASCAN IMAGE TRANS. T1/R1 & P1 SOFTWARE, Substantially Equivalent on 1987-08-12. 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: 1987-05-22
Decision date: 1987-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

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