RS-3000 ADVANCE— 510(k) K132323
Substantially EquivalentNidek Co., Ltd.
FDA 510(k) clearance K132323 for RS-3000 ADVANCE, Substantially Equivalent on 2014-02-19. Applicant: Nidek Co., Ltd..
Clearance details
- Applicant
- Nidek Co., Ltd.
- Product code
- Code OBO
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wadsworth, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.