# K853650: Auto Suture Titanium Hemostatic Clip

- Pathway: 510(k) (Traditional)
- Applicant: United States Surgical, A Division of Tyco Healthc
- Decided: Sep 19, 1985 after 16 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
No predicates in its family tree.
8 later devices descend from it; 4 cite it directly.
0 of 9 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
- K972745: Titanium Hemostatic Clip (1997), 4 descendants of its own
- K981645: Titanium Hemostatic Clip (1998), 3 descendants of its own
- K142869: Premium Surgiclip III (2014), 2 descendants of its own
- K143644: Premium Surgiclip¿; Endo Clip¿; AcuClip¿ (2015), 1 descendant of its own
- K242541: Gem Zipclip (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K853650
Methodology: https://510kreport.com/methodology