Home / 510(k) Clearances / K052195

510(k) K052195

EZ-MIO MANUAL DRIVER by Vidacare Corporation — Product Code FMI

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 2, 2005
Date Received
August 11, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Hypodermic, Single Lumen
Device Class
Class II
Regulation Number
880.5570
Review Panel
HO
Submission Type

Other clearances by Vidacare Corporation

  • K132583 — EZ-IO INTRAOSSEOUS INFUSION SYSTEM (February 11, 2014)
  • K120661 — THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE (June 3, 2012)
  • K113872 — THE ONCONTROL BONE ACCESS AND BONE BIOPSY SYSTEM BY VIDACARE (March 8, 2012)
  • K101026 — POWERED PD-IO INFUSION SYSTEM, EZ-IO HUMERAL HEAD, POWERED PH-IO (July 27, 2010)
  • K091140 — EZ-MIO DISTAL TIBIA, EZ-IO DISTAL TIBIA, VIDAPORT INTRAOSSEOUS INFUSION SYSTEM, (October 14, 2009)
  • K081713 — VERTEBRAL ACCESS SYSTEM BY VIDACARE (November 21, 2008)
  • K072045 — ONCONTROL BONE MARROW BIOPSY SYSTEM (October 22, 2007)
  • K070759 — POWERED EZ-IO PEDIATRIC BONE MARROW ASPIRATION SYSTEM (May 21, 2007)
  • K063567 — EZ-MIO STERNAL (January 26, 2007)
  • K063142 — MANUAL PD-IO; POWERED PD-IO (December 8, 2006)

Other clearances for product code FMI

  • K252886 — Pen Needle (January 6, 2026)
  • K250700 — Pen Injector Needle 32.5 (November 21, 2025)
  • K252631 — Profoject™ Disposable Needle (October 16, 2025)
  • K250724 — Intraosseous Infusion Needles (July 30, 2025)
  • K250284 — TSK SELECT™ Needle (July 24, 2025)
  • K251447 — K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB) (July 8, 2025)
  • K243309 — 27G x 1/2 TW K-Pack Surshield Needle (KN-S2713RBT) (May 29, 2025)
  • K240355 — FROG (Filter Removal of Glass) (April 18, 2025)
  • K243581 — K-Pack Enhance Needle (KH-2713RBBTC and KH-2913RBBTC) (April 4, 2025)
  • K250658 — SureFine Pen Needle (April 3, 2025)