Gebauer Medizintechnik GmbH
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K072102 | EPIVISION SL SYSTEM | January 16, 2009 |
| K041206 | EPITOME SYSTEM | September 15, 2004 |