# K152082: Vesocclude Polymer Ligating Clip

- Pathway: 510(k) (Traditional)
- Applicant: Vesocclude Medical, LLC
- Decided: Feb 26, 2016 after 214 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: 3 generations back to K922186 (1992). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030311: Hem-O-Lok XL Clip, Weck (2003) Summary page 4.
- K003337: Hem-O-Lok SMX, Model 544220; Hem-O-Lok ML, Model 544230; Hem-O-Lok MLX, Model 544240, Weck Closure Systems (2000) Summary page 4.
- K993157: Hem-O-Lok SMX Polymer Clips, Model 544220, Hem-0-Lok MLX Polymer Clips, Model 544240, Weck Closure Systems (1999) Summary page 4.
- K902108: Hem-O-Lok (TM), Edward Weck, Inc. (1990) Summary page 4.

## Indications for use
Intended Use: The Vesocclude Polymer Ligation Clips are intended for use in procedures involving ligation of vessels or tissue structures. Surgeons should apply the appropriate size clip for the size of the vessel or tissue structure to be ligated such that the clip completely encompasses the vessel or tissue structure. Contraindications: Vesocclude polymer ligation clips are not intended for use as a fallopian contraceptive tubal occlusion device. Vesocclude polymer ligation clips are contraindicated for use in ligating the renal artery during laparoscopic donor nephrectomies.

Source page: https://510kreport.com/device/K152082
Methodology: https://510kreport.com/methodology