Denver Biomedicals, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K051084 | DENVER PLEURX DRAINAGE KIT AND DENVER PLEURX VACUUM BOTTLE WITH DRAINAGE LINE | June 13, 2005 |
| K011020 | DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER | June 1, 2001 |
| K010642 | PLEURX PLEURAL CATHETER AND DRAINAGE KITS | March 20, 2001 |
| K003451 | DENVER PAK W/ DOUBLE-VALVE ASCITES SHUNT,DENVER PAK W/ SINGLE-VALVED ASCITES SHUNT, DENVER PAK, DOUB | January 2, 2001 |
| K943968 | TUNNELER | March 1, 1995 |
| K913728 | DENVER(R) PERITONEO-SUBCLAVIAN SHUNT | February 18, 1994 |
| K842139 | THE DENVER PLEURAL-PERITONEAL SHUNT | August 27, 1984 |
| K822686 | DENVER PERITONEO-VENOUS SHUNT (DP-VS) | September 21, 1982 |
| K811577 | CROUCH CORNEAL PROTECTOR | August 7, 1981 |
| K811183 | DENVER PERITONEO-VENOUS SHUNT | July 1, 1981 |