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Charger™

BOSTON SCIENTIFIC CORPORATION · Model H74939206060670 · UDI-DI 08714729804406

FGELIT Prescription
10
510(k) clearances
34,031
Adverse events (362 deaths)
0
Recalls
149
Facilities

Description

PTA Balloon Dilatation Catheter

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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.