CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI— 510(k) K031629

Substantially Equivalent

Canon USA, Inc.

FDA 510(k) clearance K031629 for CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI, Substantially Equivalent on 2003-06-06. Applicant: Canon USA, Inc..

Clearance details

Applicant: Canon USA, Inc.
Product code: Code HKI
Advisory panel: Ophthalmic
Date received: 2003-05-27
Decision date: 2003-06-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Success, NY, US

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