# K954669: Femostop, Femostop Pump

- Pathway: 510(k) (Traditional)
- Applicant: Radi Medical Systems AB
- Decided: Oct 27, 1995 after 17 days
- Product code: DXC (Clamp, Vascular)
- Device class: 2
- Regulation: 21 CFR 870.4450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
26 later devices descend from it; 2 cite it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K983471: Femostop Compression Arch, Femostop Pump, Femostop Bilateral Adapter (1999), 25 descendants of its own
- K024107: Femostop Femoral Compression System (2002), 23 descendants of its own
- K040730: Vascular Solutions D-Stat Clamp Hemostatic Clamp (2004), 17 descendants of its own
- K050146: Vascular Solutions D-Stat Clamp Accessory (2005), 16 descendants of its own
- K053300: Syvekexcel (2006), 14 descendants of its own

Source page: https://510kreport.com/device/K954669
Methodology: https://510kreport.com/methodology