Company ยท US
Denver Biomedicals, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 2005. Name variants (Inc, Corp, punctuation) are merged.
10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 13, 2005 | K051084 | DENVER PLEURX DRAINAGE KIT AND DENVER PLEURX VACUUM BOTTLE WITH DRAINAGE LINE Denver Biomedicals, Inc. | DWM |
| Jun 1, 2001 | K011020 | DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER Denver Biomedicals, Inc. | KPM |
| Mar 20, 2001 | K010642 | PLEURX PLEURAL CATHETER AND DRAINAGE KITS Denver Biomedicals, Inc. | DWM |
| Jan 2, 2001 | K003451 | DENVER PAK W/ DOUBLE-VALVE ASCITES SHUNT,DENVER PAK W/ SINGLE-VALVED ASCITES SHUNT, DENVER PAK, DOUBLED-VALVED ASCITES T Denver Biomedicals, Inc. | KPM |
| Mar 1, 1995 | K943968 | TUNNELER Denver Biomedicals, Inc. | MDM |
| Feb 18, 1994 | K913728 | DENVER(R) PERITONEO-SUBCLAVIAN SHUNT Denver Biomedicals, Inc. | KPM |
| Aug 27, 1984 | K842139 | THE DENVER PLEURAL-PERITONEAL SHUNT Denver Biomedicals, Inc. | KPM |
| Sep 21, 1982 | K822686 | DENVER PERITONEO-VENOUS SHUNT (DP-VS) Denver Biomedicals, Inc. | KPM |
| Aug 7, 1981 | K811577 | CROUCH CORNEAL PROTECTOR Denver Biomedicals, Inc. | HOY |
| Jul 1, 1981 | K811183 | DENVER PERITONEO-VENOUS SHUNT Denver Biomedicals, Inc. | KPM |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||