# K901303: Horizon Surgical Ligating and Marking Clip

- Pathway: 510(k) (Traditional)
- Applicant: Horizon Surgical, Inc.
- Decided: Jun 5, 1990 after 77 days
- Product code: DSS (Clip, Vascular)
- Device class: 2
- Regulation: 21 CFR 870.3250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K230966: angiOCCLUDE Ligating Clips (2023), 0 descendants of its own
- K091060: Vesocclude Ligating Clip (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K901303
Methodology: https://510kreport.com/methodology