Laser-Optik-Systeme GmbH & Co. KG
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K972056 | STANDARD ENDOSCOPE | July 30, 1997 |
| K950712 | PORTABLE ENDOSCOPY SYSTEM | May 14, 1996 |
| K952028 | COLD LIGHT SOURCE LOS XL-A 100 | July 27, 1995 |
| K951829 | COLD LIGHT SOURCE LOS 150 | July 10, 1995 |