# K000221: Series 7700 Mobile C-Arm, Compact 7700 Mobile C-Arm, Compact 7700 Plus Mobile C-Arm

- Pathway: 510(k) (Abbreviated)
- Applicant: Ge Dec Medical Systems
- Decided: Apr 11, 2000 after 78 days
- Product code: OWB (Interventional Fluoroscopic X-Ray System)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K051490: GE Oec Everview 7500 (2005), 0 descendants of its own

## Recalls of this device
- Sep 28, 2007 · Not classified · Z-0717-2008: Unnecessary operator exposure; X-ray machine may allow unwanted x-ray exposure to the operator.

Source page: https://510kreport.com/device/K000221
Methodology: https://510kreport.com/methodology