Loseff Medical Designers, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K802025 | BALLOON RETENTION CHEST CATHETER | September 26, 1980 |
| K801349 | LOSEFF BALLOON TYPE SELF-RETENTION WOUND | August 7, 1980 |