# Ge Dec Medical Systems

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 10 (1994–2000): 10 510(k) clearances
- Product codes: OWB (5), JAA (3), OXO (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 7 (1 its own)
- Recalls linked to its devices: 24 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Mallinckrodt Group, Inc.: 2 (https://510kreport.com/company/mallinckrodt-group)

## Firms that cite its devices most
- Ge Oec Medical Systems, Inc.: 2 (https://510kreport.com/company/ge-oec-medical-systems)
- Pck Electronic Industry and Trade Co, Ltd.: 1 (https://510kreport.com/company/pck-electronic-industry-and-trade)
- Stereotaxis, Inc.: 1 (https://510kreport.com/company/stereotaxis)
- Ge Hangwei Medical Systems Co., Ltd.: 1 (https://510kreport.com/company/ge-hangwei-medical-systems)
- Lunar Corp.: 1 (https://510kreport.com/company/lunar)

## Its most-cited devices
- K940295: Uroview Model 2600 (1994), cited by 2
- K974355: Interventional Mobile Digital Imaging System (Herein Called Imdis) (1998), cited by 2
- K951765: Series 6600 Digital Mobile C-Arm (1995), cited by 1
- K992506: Mini 6800 Digital Mobile C-Arm (1999), cited by 1
- K000221: Series 7700 Mobile C-Arm, Compact 7700 Mobile C-Arm, Compact 7700 Plus Mobile C-Arm (2000), cited by 1

## Recent decisions
- K000221: Series 7700 Mobile C-Arm, Compact 7700 Mobile C-Arm, Compact 7700 Plus Mobile C-Arm (Apr 11, 2000)
- K993687: Uroview 2800 (Dec 21, 1999)
- K992506: Mini 6800 Digital Mobile C-Arm (Aug 19, 1999)
- K974355: Interventional Mobile Digital Imaging System (Herein Called Imdis) (Feb 17, 1998)
- K970063: Series 7600 Mobile Digital C-Arm (Mar 11, 1997)
- K963952: Series 9600 Mobile Digital Imaging System (Dec 23, 1996)
- K950781: Compact 7600 (Jun 5, 1995)
- K951765: Series 6600 Digital Mobile C-Arm (May 11, 1995)

Source page: https://510kreport.com/company/ge-dec-medical-systems