Modified Formed-Extension Mahurkar Dual Lumen Cath

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K880583 ↗

FDA Product Code

MPB

Device Class

Class II

Regulation

21 CFR Part 876.5540

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

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  Class I

  FDA 510(k) K911751 Active Cleared 29 May 1991

• Patient by-Pass

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See all devices from Quinton, Inc. →