Vantage Peripheral Dilatation Catheter

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K965183 ↗

FDA Product Code

LIT

Device Class

Class II

Regulation

21 CFR Part 870.1250

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

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See all devices from Guidant Corp. →