Company ยท US
Denver Biomedical, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2005. Name variants (Inc, Corp, punctuation) are merged.
5510(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 |
|---|---|---|---|
| Nov 15, 2005 | K051711 | PLEURX PERITONEAL CATHETER KIT AND PLEURX DRAINAGE KITS Denver Biomedical, Inc. | PNG |
| Oct 6, 2005 | K052436 | PLEURX PLEURAL CATHETER KIT, MODEL 50-7000 Denver Biomedical, Inc. | DWM |
| Oct 4, 2001 | K012235 | DENVER PLEURAL EFFUSION SHUNT AND DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER Denver Biomedical, Inc. | KPM |
| Jul 12, 2001 | K011862 | DENVER ASCITES SHUNT AND PERCUTANEOUS ACCESS KIT WITH ASCITIES SHUNT Denver Biomedical, Inc. | KPM |
| Jun 28, 2001 | K011831 | MODIFICATION TO PLEURX PLEURAL CATHETER AND DRAINAGE KITS Denver Biomedical, Inc. | DWM |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||