ECKHARDT TEMPORARY KERATOPROSTHESIS— 510(k) K902491
Substantially EquivalentDutch Ophthalmic USA, Inc.
FDA 510(k) clearance K902491 for ECKHARDT TEMPORARY KERATOPROSTHESIS, Substantially Equivalent on 1990-06-26. Applicant: Dutch Ophthalmic USA, Inc..
Clearance details
- Applicant
- Dutch Ophthalmic USA, Inc.
- Product code
- Code MLP
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kingston, NH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.