# K951765: Series 6600 Digital Mobile C-Arm

- Pathway: 510(k) (Traditional)
- Applicant: Ge Dec Medical Systems
- Decided: May 11, 1995 after 24 days
- Product code: OXO (Image-Intensified Fluoroscopic X-Ray System, Mobile)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: none
- 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. The FDA summary names its predicate without a number.
- (no number) OEC Medical Systems, Inc. - Series 9600 Mobile Digital Imaging System: named in the summary without a submission number
- (no number) FluoroScan Imaging Systems, Inc. - FluoroScan Mini C-arm: named in the summary without a submission number
- (no number) XiTec Incorporated - XiScan Mini C-arm: named in the summary without a submission number

## Most influential descendants
- K960907: ORCA (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K951765
Methodology: https://510kreport.com/methodology