Landmark Dual-Lumen Midline Catheter System

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K912165 ↗

FDA Product Code

FOZ

Device Class

Class II

Regulation

21 CFR Part 880.5200

Advisory Committee

General Hospital

FDA Decision

SEKD

• Versacath Selectalumen Inner Catheter

  Class II

  FDA 510(k) K920133 Active Cleared 26 Mar 1992

• Intropeel V

  Class II

  FDA 510(k) K931218 Active Cleared 22 Sep 1993

• Safe-Picc Catheter

  Class II

  FDA 510(k) K930048 Active Cleared 12 May 1994

• Streamline Vascular Access Device

  Class II

  FDA 510(k) K896774 Active Cleared 27 Dec 1989

• Landmark Venous Access Drive (Additional Sizes)

  Class II

  FDA 510(k) K883980 Active Cleared 5 Dec 1988

• Menlo Care Urinary Diversion Stent

  Class II

  FDA 510(k) K933941 Active Cleared 31 Mar 1994

See all devices from Menlo Care, Inc. →