CANON AUTOREFRACTOMETER R-22— 510(k) K883200
Substantially EquivalentCanon USA, Inc.
FDA 510(k) clearance K883200 for CANON AUTOREFRACTOMETER R-22, Substantially Equivalent on 1988-08-18. Applicant: Canon USA, Inc..
Clearance details
- Applicant
- Canon USA, Inc.
- Product code
- Code HKO
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jericho, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.