Specialities Remeex International, S.L.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K063136 | NEEDLELESS SLING | December 19, 2006 |
| K062341 | MALE REMEEX SYSTEM | November 2, 2006 |
| K033310 | REMEEX SYSTEM FOR URINARY INCONTINENCE | January 15, 2004 |