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JETi™

ABBOTT VASCULAR INC. · Model WV062F · UDI-DI 08717648353291

QEZ Prescription
10
510(k) clearances
83
Adverse events (25 deaths)
0
Recalls
49
Facilities

Description

JETi™ 6F 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.