# K081740: Hemoband, Models HB-NS and HB-NSXL

- Pathway: 510(k) (Traditional)
- Applicant: Innovations For Access, Inc.
- Decided: Mar 12, 2009 after 266 days
- Product code: KOC (Accessories, Blood Circuit, Hemodialysis)
- Device class: 2
- Regulation: 21 CFR 876.5820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 2 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K142122: Radar Vascular Compression Device (2014), 3 descendants of its own
- K142359: Vasc Band hemostat (2014), 3 descendants of its own
- K162988: PreludeSYNC Radial Compression Device (2017), 1 descendant of its own
- K151363: Zephyr Vascular Compression Device (2015), 1 descendant of its own
- K262086: PreludeSYNC™ Radial Compression Device (2026), 0 descendants of its own

## Indications for use
The HemoBand is used to provide pressure hemostasis of arterial, venous and dialysis access needle puncture sites.

Source page: https://510kreport.com/device/K081740
Methodology: https://510kreport.com/methodology