FDA Device Intelligence
Home › CAREFUSION 2200, INC › Denver

Denver

CAREFUSION 2200, INC · Model 42-2005 · UDI-DI 10885403076015

KPM Prescription
10
510(k) clearances
126
Adverse events (7 deaths)
0
Recalls
7
Facilities

Description

Denver Ascites Shunt, 15.5 Fr - Ascites Shunt Single-Valved

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.