Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Denver Biomedical, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Nov 15, 2005: PLEURX PERITONEAL CATHETER KIT AND PLEURX DRAINAGE KITS.
| Nov 15, 2005 | PLEURX PERITONEAL CATHETER KIT AND PLEURX DRAINAGE KITSK051711 · PNG | 510(k) clearances |
| Oct 6, 2005 | PLEURX PLEURAL CATHETER KIT, MODEL 50-7000K052436 · DWM | 510(k) clearances |
| Oct 4, 2001 | DENVER PLEURAL EFFUSION SHUNT AND DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBERK012235 · KPM | 510(k) clearances |
| Jul 12, 2001 | DENVER ASCITES SHUNT AND PERCUTANEOUS ACCESS KIT WITH ASCITIES SHUNTK011862 · KPM | 510(k) clearances |
| Jun 28, 2001 | MODIFICATION TO PLEURX PLEURAL CATHETER AND DRAINAGE KITSK011831 · DWM | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
