# Denver Biomedicals, Inc.

- Location (FDA's records): Golden, CO
- FDA decisions: 10 (1981–2005): 10 510(k) clearances
- Product codes: KPM (6), DWM (2), MDM (1), HOY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Pfm Medical, Inc.: 2 (https://510kreport.com/company/pfm-medical)
- Bard Access Systems, Inc.: 2 (https://510kreport.com/company/bard-access-systems)
- Denver Biomaterials, Inc.: 1 (https://510kreport.com/company/denver-biomaterials)
- Care Fusion: 1 (https://510kreport.com/company/care-fusion)
- Pleural Dynamics, Inc.: 1 (https://510kreport.com/company/pleural-dynamics)

## Its most-cited devices
- K051084: Denver Pleurx Drainage Kit and Denver Pleurx Vacuum Bottle with Drainage Line (2005), cited by 3
- K010642: Pleurx Pleural Catheter and Drainage Kits (2001), cited by 2
- K913728: Denver (R) Peritoneo-Subclavian Shunt (1994), cited by 1
- K822686: Denver Peritoneo-Venous Shunt (DP-VS) (1982), cited by 1

## Recent decisions
- 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, Doubled-Valved Ascites T (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)

Source page: https://510kreport.com/company/denver-biomedicals