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PowerPICC SOLO

Bard Access Systems, Inc. · Model CK000643 · UDI-DI 00801741127915

LJS Prescription
10
510(k) clearances
37,016
Adverse events (128 deaths)
0
Recalls
88
Facilities

Description

Catheter Placement Kit

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

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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.