Schwind Eye-Tech-Solutions GmbH & Co. KG
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K082043 | CARRIAZO-PENDULAR MICROKERATOME | August 1, 2008 |
| K032910 | CARRIAZO PENDULAR | August 30, 2004 |