POWERED EZ-IO PEDIATRIC BONE MARROW ASPIRATION SYSTEM— 510(k) K070759
Substantially EquivalentVidacare Corporation
FDA 510(k) clearance K070759 for POWERED EZ-IO PEDIATRIC BONE MARROW ASPIRATION SYSTEM, Substantially Equivalent on 2007-05-21. Applicant: Vidacare Corporation. Device class: 2.
Clearance details
- Applicant
- Vidacare Corporation
- Product code
- Code FCF
- Device class
- Class 2
- Regulation
- 21 CFR 876.1075
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
Recent devices under product code FCF
view allMore clearances from Vidacare Corporation
view all- 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
Data sourced from openFDA. This site is unofficial and independent of the FDA.