# K142122: Radar Vascular Compression Device

- Pathway: 510(k) (Abbreviated)
- Applicant: Advanced Vascular Dynamics
- Decided: Dec 4, 2014 after 122 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). 8 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 12 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 4.
- K081740: Hemoband, Models HB-NS and HB-NSXL, Innovations For Access, Inc. (2009) Summary page 4.

## Most influential descendants
- K151363: Zephyr Vascular Compression Device (2015), 1 descendant of its own
- K170958: ChitoPulse 9in / 23 cm, ChitoPulse 12in / 30.5 cm, ChitoPulse 15in / 38 cm (2017), 0 descendants of its own
- K153259: VasoStat Hemostasis Device (2016), 0 descendants of its own

## Indications for use
The RadAR™ Vascular Compression Devices are indicated for use by medical professionals to promote hemostasis following a catheterization or other puncture into a blood vessel in a patient’s arm or leg, including: radial, brachial, dorsalis pedis or tibial blood vessels, arterial or venous line or sheath removal, hemodialysis, and in patients on anticoagulation therapy.

Source page: https://510kreport.com/device/K142122
Methodology: https://510kreport.com/methodology