# K925149: Auto Suture Endoscopic Knot Pusher

- Pathway: 510(k) (Traditional)
- Applicant: United States Surgical, A Division of Tyco Healthc
- Decided: Jan 26, 1993 after 105 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K994087: Superstitch (2000), 2 descendants of its own
- K012865: Superstitch Vascular Suturing Device (2001), 1 descendant of its own
- K020940: Superstitch Vascular Suturing Device, 6 French, Models 06-15-00X; Mid-Length 06-25-00X (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K925149
Methodology: https://510kreport.com/methodology