Lemaitre Biliary Catheter

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K992941 ↗

FDA Product Code

LQR

Device Class

Class II

Regulation

21 CFR Part 876.5010

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Lemaitre Irrigation Catheter

  Class II

  FDA 510(k) K992933 Active Cleared 8 Mar 2000

• LeMaitre Occlusion Catheter

  Class II

  FDA 510(k) K992942 Active Cleared 13 Apr 2000

• Lemaitre-Bookwalter Vessel Devices

  Class II

  FDA 510(k) K912548 Active Cleared 18 Sep 1991

• Lemaitre Embolectomy Catheter Open recall

  Class II

  FDA 510(k) K992368 Active Cleared 9 Dec 1999

• Lemaitre Balloon Catheter with Irrigation

  Class II

  FDA 510(k) K992940 Active Cleared 22 Feb 2000

• The Samuels Retrograd Valvulotome

  Class II

  FDA 510(k) K932009 Active Cleared 21 Sep 1993

See all devices from Vascutech, Inc. →