CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI— 510(k) K031629
Substantially EquivalentCanon 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.. 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
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lake Success, NY, US
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