Lockbox for Use with Medfusion 3000 Series Pumps

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K091181 ↗

FDA Product Code

MRZ

Device Class

Class II

Regulation

21 CFR Part 880.5725

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Deltec Cozmo Insulin Infusion Pump with Cozmonitor Blood Glucose Meter, Models 21-1815, 21-1816, 21-1817

  Class II

  FDA 510(k) K062323 Active Cleared 1 Nov 2006

• Smith Medical Peel-Away Sheath Introducers

  Class II

  FDA 510(k) K112407 Active Cleared 9 Feb 2012

• Power Port-a-Cath, Cath II, and P.A.S. Port T2 Power P.A.C. Implantable Venous Access Systems and Power Gripper Plus

  Class II

  FDA 510(k) K072657 Active Cleared 14 Dec 2007

• Port-A-Cath, Port-a-Cath II, Proport and P.A.S. Port Implantable Venous Access Systems with Dual Layer Catheter

  Class II

  FDA 510(k) K060036 Active Cleared 17 May 2006

• Cadd Administration Set with Flow Stop, Medication Cassette Reservoir with Flow Stop and Extension Set Open recall

  Class II

  FDA 510(k) K040636 Active Cleared 19 May 2004

• Gripper Micro Needle

  Class II

  FDA 510(k) K072059 Active Cleared 1 Nov 2007

See all devices from Smiths Medical MD, Inc. →