NON-MYDRIATIC RETINAL CAMERA, CR-45UAF— 510(k) K911439

Name: FDA 510(k) clearance K911439
Creator: U.S. Food and Drug Administration
Published: 1991-06-17

Substantially Equivalent

Canon USA, Inc.

FDA 510(k) clearance K911439 for NON-MYDRIATIC RETINAL CAMERA, CR-45UAF, Substantially Equivalent on 1991-06-17. Applicant: Canon USA, Inc.. Device class: 2.

Clearance details

Applicant: Canon USA, Inc.
Product code: Code HKI
Device class: Class 2
Regulation: 21 CFR 886.1120
Advisory panel: Ophthalmic
Date received: 1991-04-02
Decision date: 1991-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tokyo 146, JP

Download summary PDF View on FDA.gov ↗

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