Percutaneous Systems, Incorporated
Percutaneous Systems, Incorporated appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 22, 2009.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K090485 | COAXIAL ACCORDION ERCP DEVICE, MODELS C0AC19001, COAC20005, COAC22003 | July 22, 2009 |
| K061766 | EXPRESSWAY INTERMITTENT CATHETER | March 9, 2007 |
| K052298 | CYSTOGLIDE INTRODUCER SHEATH | December 12, 2006 |
| K052048 | ACCORDION | September 13, 2005 |
| K042531 | UPDATED SLIP UROLOGY INTRODUCER SHEATH | February 1, 2005 |