Denver Biomedicals, Inc.
Denver Biomedicals, Inc. has 0 FDA recalls, 0 inspections, 10 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Jun 13, 2005
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 10 | Oct 4, 2026 | Not stated | Current |
| Inspections | 0 | Oct 25, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K051084 | DENVER PLEURX DRAINAGE KIT AND DENVER PLEURX VACUUM BOTTLE WITH DRAINAGE LINE | Jun 13, 2005 |
| K011020 | DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER | Jun 1, 2001 |
| K010642 | PLEURX PLEURAL CATHETER AND DRAINAGE KITS | Mar 20, 2001 |
| K003451 | DENVER PAK W/ DOUBLE-VALVE ASCITES SHUNT,DENVER PAK W/ SINGLE-VALVED ASCITES SHUNT, DENVER PAK… | Jan 2, 2001 |
| K943968 | TUNNELER | Mar 1, 1995 |
| K913728 | DENVER(R) PERITONEO-SUBCLAVIAN SHUNT | Feb 18, 1994 |
| K842139 | THE DENVER PLEURAL-PERITONEAL SHUNT | Aug 27, 1984 |
| K822686 | DENVER PERITONEO-VENOUS SHUNT (DP-VS) | Sep 21, 1982 |
| K811577 | CROUCH CORNEAL PROTECTOR | Aug 7, 1981 |
| K811183 | DENVER PERITONEO-VENOUS SHUNT | Jul 1, 1981 |