Stebar Instrument 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 |
|---|
| K952266 | SCHROEDER ORAL/NASAL DIRECTIONAL STYLETTE | June 12, 1995 |
| K935797 | SCHROEDER ORAL/NASAL DIRECTIONAL STYLETTE | January 12, 1994 |