# K032885: Vidaport Intraosseous Infusion System

- Pathway: 510(k) (Traditional)
- Applicant: Vidacare Corporation
- Decided: Mar 10, 2004 after 176 days
- Product code: FMI (Needle, Hypodermic, Single Lumen)
- Device class: 2
- Regulation: 21 CFR 880.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K981853 (1998). 1 ancestor in all.
38 later devices descend from it; 8 cite it directly.
0 of 40 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K981853: Bone Injection Gun (B.I.G.) Device, Waismed, Ltd. (1998) Summary page 1.

## Most influential descendants
- K043490: PD-IO Disposable Intraosseous Infusion Needle (2005), 16 descendants of its own
- K062833: Powered EZ-IO Bone Marrow Aspiration System (2006), 14 descendants of its own
- K052195: EZ-Mio Manual Driver (2005), 13 descendants of its own
- K052408: EZ-IO (2005), 9 descendants of its own
- K072045: Oncontrol Bone Marrow Biopsy System (2007), 7 descendants of its own

## Indications for use
The VidaPort provides intraosseous access in the proximal tibia, as an alternative to IV access during emergencies. The device is for use in adult patients only.

Source page: https://510kreport.com/device/K032885
Methodology: https://510kreport.com/methodology