Vidacare Corporation
FDA 510(k) medical device clearances.
Top product codes for Vidacare Corporation
Recent clearances by Vidacare Corporation
- K132583 — EZ-IO INTRAOSSEOUS INFUSION SYSTEM
- K120661 — THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE
- K113872 — THE ONCONTROL BONE ACCESS AND BONE BIOPSY SYSTEM BY VIDACARE
- K101026 — POWERED PD-IO INFUSION SYSTEM, EZ-IO HUMERAL HEAD, POWERED PH-IO
- K091140 — EZ-MIO DISTAL TIBIA, EZ-IO DISTAL TIBIA, VIDAPORT INTRAOSSEOUS INFUSION SYSTEM, EZ-IO
- K081713 — VERTEBRAL ACCESS SYSTEM BY VIDACARE
- K072045 — ONCONTROL BONE MARROW BIOPSY SYSTEM
- K070759 — POWERED EZ-IO PEDIATRIC BONE MARROW ASPIRATION SYSTEM
- K063567 — EZ-MIO STERNAL
- K063142 — MANUAL PD-IO; POWERED PD-IO
- K062956 — EZ-MIO, EZ-IO DISTAL TIBIA
- K062833 — POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM
- K062422 — HUMERAL HEAD, MANUAL DRIVER
- K061771 — EZ-CONNECT
- K052408 — EZ-IO
- K052195 — EZ-MIO MANUAL DRIVER
- K051992 — POWERED PD-IO INTRAOSSEOUS INFUSION SYSTEM
- K043490 — PD-IO DISPOSABLE INTRAOSSEOUS INFUSION NEEDLE
- K032885 — VIDAPORT INTRAOSSEOUS INFUSION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.