KODAK PORTABLE IDENTIFICATION CAMERA— 510(k) K890467

Name: FDA 510(k) clearance K890467
Creator: U.S. Food and Drug Administration
Published: 1989-02-16

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K890467 for KODAK PORTABLE IDENTIFICATION CAMERA, Substantially Equivalent on 1989-02-16. Applicant: Eastman Kodak Company. Device class: 1.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code JAC
Device class: Class 1
Regulation: 21 CFR 892.1640
Advisory panel: Radiology
Date received: 1989-01-31
Decision date: 1989-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

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