Denver Biomedicals, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K051084 | DENVER PLEURX DRAINAGE KIT AND DENVER PLEURX VACUUM BOTTLE WITH DRAINAGE LINE | DWM | 2005-06-13 | View |
| 510(k) | K011020 | DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER | KPM | 2001-06-01 | View |
| 510(k) | K010642 | PLEURX PLEURAL CATHETER AND DRAINAGE KITS | DWM | 2001-03-20 | View |
| 510(k) | K003451 | DENVER PAK W/ DOUBLE-VALVE ASCITES SHUNT,DENVER PAK W/ SINGLE-VALVED ASCITES SHUNT, DENVER PAK, DOUBLED-VALVED ASCITES T | KPM | 2001-01-02 | View |
| 510(k) | K943968 | TUNNELER | MDM | 1995-03-01 | View |
| 510(k) | K913728 | DENVER(R) PERITONEO-SUBCLAVIAN SHUNT | KPM | 1994-02-18 | View |
| 510(k) | K842139 | THE DENVER PLEURAL-PERITONEAL SHUNT | KPM | 1984-08-27 | View |
| 510(k) | K822686 | DENVER PERITONEO-VENOUS SHUNT (DP-VS) | KPM | 1982-09-21 | View |
| 510(k) | K811577 | CROUCH CORNEAL PROTECTOR | HOY | 1981-08-07 | View |
| 510(k) | K811183 | DENVER PERITONEO-VENOUS SHUNT | KPM | 1981-07-01 | View |
No matching devices.
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