FDA Device Intelligence
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Shunt, Peritoneal

FDA product code KPM · Class 2 · Gastroenterology, Urology

17
Registered devices
126
Adverse events
0
Recalls
19
510(k) clearances

Devices with this code

N/A — CAREFUSION 2200, INCDenver — CAREFUSION 2200, INCDenver — CAREFUSION 2200, INCN/A — CAREFUSION 2200, INCDenver — CAREFUSION 2200, INCN/A — CAREFUSION 2200, INCCurve — CAREFUSION 2200, INCDenver — CAREFUSION 2200, INCDenver — CAREFUSION 2200, INCDenver — CAREFUSION 2200, INCDenver — CAREFUSION 2200, INCCurve — CAREFUSION 2200, INCCurve — CAREFUSION 2200, INCDenver — CAREFUSION 2200, INCCurve — CAREFUSION 2200, INCCurve — CAREFUSION 2200, INCDenver — CAREFUSION 2200, INC

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.