DIGITAL RETINAL CAMERA, CR-1 MARK II— 510(k) K090466
Substantially EquivalentCanon, Inc.
FDA 510(k) clearance K090466 for DIGITAL RETINAL CAMERA, CR-1 MARK II, Substantially Equivalent on 2009-03-23. Applicant: Canon, Inc.. Device class: 2.
Clearance details
- Applicant
- Canon, Inc.
- Product code
- Code HKI
- Device class
- Class 2
- Regulation
- 21 CFR 886.1120
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lake Success, NY, US
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