Percutaneous Systems, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K102887 | ACCORDION STONE MANAGEMENT DEVICE MODEL AC281205 AND AC3814510 | May 16, 2011 |
| K082803 | COAXIAL ACCORDION STONE MANAGEMENT DEVICE, MODEL: COAC12005 - COA20015 | November 13, 2008 |
| K052134 | CYSTOGLIDE DILATING INTRODUCER SHEATH | September 22, 2005 |
| K042877 | MICROVERTER URETERAL ACCESS SHEATH | November 16, 2004 |
| K040519 | SLIP UROLOGY CATHETER | May 20, 2004 |
| K040520 | SLIP UROLOGY INTRODUCER SHEATH | May 20, 2004 |