Home › CAREFUSION 2200, INC › Curve

Curve

CAREFUSION 2200, INC · Model 42-2025 · UDI-DI 10885403222672

KPM Prescription

510(k) clearances

126

Adverse events (7 deaths)

Recalls

Facilities

Description

Curve Ascites Shunt PAK 15.5Fr, Ascites Shunt Percutaneous Access Kit / 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 key Read 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.