DIGITAL RETINAL CAMERA, CR-1 MARK II— 510(k) K090466

Substantially Equivalent

Canon, Inc.

FDA 510(k) clearance K090466 for DIGITAL RETINAL CAMERA, CR-1 MARK II, Substantially Equivalent on 2009-03-23. Applicant: Canon, Inc..

Clearance details

Applicant: Canon, Inc.
Product code: Code HKI
Advisory panel: Ophthalmic
Date received: 2009-02-21
Decision date: 2009-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Success, NY, US

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