# K123041: Vasostat Hemostasis Device

- Pathway: 510(k) (Traditional)
- Applicant: Forge Medical, Inc.
- Decided: May 29, 2013 after 243 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
Longest line of descent: 4 generations back to K984177 (1998). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K092503: Radar Vascular Compression Devices, Advanced Vascular Dynamics (2009) Summary page 1.
- K070423: TR Band, Terumo Medical Corp. (2007) Summary page 1.

## Cited in the summary but kept off the family tree
- D147574: VasoStat Hemostasis Device. Number could not be read Summary page 1.

## Most influential descendants
- K153259: VasoStat Hemostasis Device (2016), 0 descendants of its own

## Indications for use
The VasoStat"" Hemostasisbevice is indicated for use by medical professionals to promote hernostasis following a catheterization or other puncture into a blood vessel in a patient's arm, including radial artery catheterization, arterial or venous line removal, hemodialysis, and in patients on anticoagulation therapy.

Source page: https://510kreport.com/device/K123041
Methodology: https://510kreport.com/methodology