# K140932: Amsel Occluder Device

- Pathway: 510(k) (Traditional)
- Applicant: Amsel Medical Corporation
- Decided: Jan 23, 2015 after 287 days
- Product code: FZP (Clip, Implantable)
- Device class: 2
- Regulation: 21 CFR 878.4300
- 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 K830503 (1983). 4 ancestors in all.
2 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)
- K032238: Twister Superelastic Ligating Clip and Applier, Neurosel (Medical) Limited (2003) Summary page 5.
- K834267: Ligaclip Metallic Ligating Clip, ETHICON, Inc. (1984) Summary page 5.

## Most influential descendants
- K260677: Vessel Closure Device (VCD177213P) (2026), 0 descendants of its own
- K180650: Amsel Endo Occluder (2018), 0 descendants of its own

## Indications for use
The Amsel Occluder Device is intended for use in open general surgery procedures on tubular structures or vessels wherever a metal ligating clip is indicated and within the size range of 2.0mm to 7.0mm diameter.

Source page: https://510kreport.com/device/K140932
Methodology: https://510kreport.com/methodology