# K944350: SC 6000/ SC 6000P/ R50

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Apr 10, 1995 after 216 days
- Product code: DSI (Detector And Alarm, Arrhythmia)
- Device class: 2
- Regulation: 21 CFR 870.1025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
248 later devices descend from it; 2 cite it directly.
0 of 249 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
- K955743: Siemens SC 6000/SC 6000 P Portable Bedside Monitoring System (1996), 247 descendants of its own
- K993974: Siemens Infinity SC 6002XL Portable Patient Monitor (2000), 246 descendants of its own
- K033600: Infinity Gammaxl (2003), 244 descendants of its own
- K040188: Infinity Gammaxl and SC 6802XL with the Scio Gas Module (2004), 241 descendants of its own
- K051628: Infinity Monitors with Scio Modifications (2005), 230 descendants of its own

Source page: https://510kreport.com/device/K944350
Methodology: https://510kreport.com/methodology