Quickcat Extraction Catheter, Model 60090-01

• • Terminated Z-2190-2010 FDA Unclassified (pre-2012) ·initiated 1 Jul 2010 ·on shared 510(k) K073519

  Guidewire lumen may be occluded, preventing guidewire insertion into the catheter.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

510(k) Number

K073519 ↗

FDA Product Code

QEZ

Device Class

Class II

Regulation

21 CFR Part 870.5150

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K091499 Active Cleared 22 Oct 2009

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