Denver Biomedicals, Inc.
Denver Biomedicals, Inc. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 2005.
Top product codes for Denver Biomedicals, Inc.
Recent clearances by Denver Biomedicals, Inc.
- K051084 — DENVER PLEURX DRAINAGE KIT AND DENVER PLEURX VACUUM BOTTLE WITH DRAINAGE LINE
- K011020 — DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER
- K010642 — PLEURX PLEURAL CATHETER AND DRAINAGE KITS
- K003451 — DENVER PAK W/ DOUBLE-VALVE ASCITES SHUNT,DENVER PAK W/ SINGLE-VALVED ASCITES SHUNT, DENVER PAK, DOUBLED-VALVED ASCITES T
- K943968 — TUNNELER
- K913728 — DENVER(R) PERITONEO-SUBCLAVIAN SHUNT
- K842139 — THE DENVER PLEURAL-PERITONEAL SHUNT
- K822686 — DENVER PERITONEO-VENOUS SHUNT (DP-VS)
- K811577 — CROUCH CORNEAL PROTECTOR
- K811183 — DENVER PERITONEO-VENOUS SHUNT
Data sourced from openFDA. This site is unofficial and independent of the FDA.