Mpathy Medical Devices, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K092203 | OMNISURE URETHRAL SLING, MODEL OTK52 | August 12, 2009 |
| K092207 | RESTORELLE POLYPROPYLENE MESH | August 4, 2009 |
| K091180 | MINITAPE URETHRAL SLING | July 14, 2009 |
| K073647 | MINITAPE EXTRA URETHRAL SLING | March 3, 2008 |
| K073646 | MINITAPE URETHRAL SLING | February 25, 2008 |
| K053361 | MODIFICATION TO: MINIMESH POLYPROPYLENE MESH | February 6, 2006 |
| K041632 | MINIMESH POLYPROPYLENE MESH | November 17, 2004 |