# K040615: Compressar Supercomfort Disc and Strongarm Supercomfort System

- Pathway: 510(k) (Special)
- Applicant: Advanced Vascular Dynamics
- Decided: Jun 1, 2004 after 84 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.
17 later devices descend from it; 3 cite it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) CompressAR Universal System CompressAR Comfort Disc: named in the summary without a submission number

## Most influential descendants
- K053300: Syvekexcel (2006), 14 descendants of its own
- K061219: D-Stat Dry Hemostatic Bandage (2006), 13 descendants of its own
- K090620: Quikclot Inteventional, Model P/N 182 (2009), 5 descendants of its own
- K072890: Stasilon FR (2007), 5 descendants of its own
- K142363: Nustat, Nustat XR (2015), 4 descendants of its own

## Indications for use
This device is indicated for use to provide hemostasis of the femoral vascular access site during and following catheterization or cannulation procedures.

Source page: https://510kreport.com/device/K040615
Methodology: https://510kreport.com/methodology