# K091519: Haemoband Multi-Ligator

- Pathway: 510(k) (Traditional)
- Applicant: Haemoband Surgical, Ltd.
- Decided: Jul 28, 2009 after 67 days
- Product code: FHN (Ligator, Hemorrhoidal)
- Device class: 2
- Regulation: 21 CFR 876.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K963166 (1997). 3 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070881: Lem Hemorrhoidal Ligator, Models a.5650, a.5660, Sapimed S.P.A. (2007) Summary page 2.
- K000297: Erchinger Hemorrhoidal Ligators: Suction Ligators, Mod. Erchinger, Rudd, Mcgivney Mod. Erchinger, Erchinger Medizintecnik (2000) Summary page 2.

## Most influential descendants
- K131282: Nexus Hemorrhoid Ligator (2013), 1 descendant of its own
- K150718: Wi-3 HAL-RAR System (2015), 0 descendants of its own
- K093497: THD Bandy (2010), 0 descendants of its own

## Indications for use
The Haemoband Multi-Ligator includes suction and ligation capabilities. The ligator is used to cut off the blood flow to hemorrhoidal tissue by means of a ligature or ring placed around the hemorrhoid base. It is for use only by trained medical personnel.

Source page: https://510kreport.com/device/K091519
Methodology: https://510kreport.com/methodology