NON-MYDRIATIC RETINAL CAMERA, CR-45UAF— 510(k) K911439
Substantially EquivalentCanon USA, Inc.
FDA 510(k) clearance K911439 for NON-MYDRIATIC RETINAL CAMERA, CR-45UAF, Substantially Equivalent on 1991-06-17. Applicant: Canon USA, Inc..
Clearance details
- Applicant
- Canon USA, Inc.
- Product code
- Code HKI
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tokyo 146, JP
Data sourced from openFDA. This site is unofficial and independent of the FDA.