Innovative Surgical Devices Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K926337 | BONE LAVAGE SYSTEM | June 11, 1993 |
| K884404 | HERNIASTAT | November 8, 1988 |