Cpi Lead Adapters, Models 6017, 6018 and 6020

No FDA recalls on record, checked 12 Oct 2026.

510(k) Number

K041574 ↗

FDA Product Code

DTD

Models / Variants

6017

6018

6020

Device Class

Class II

Regulation

21 CFR Part 870.3620

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

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See all devices from Guidant Corp. →