# K903206: Auto Suture (R) Endoscopic Scissors

- Pathway: 510(k) (Traditional)
- Applicant: United States Surgical, A Division of Tyco Healthc
- Decided: Oct 17, 1990 after 89 days
- Product code: HET (Laparoscope, Gynecologic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1720
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
14 later devices descend from it; 1 cites it directly.
0 of 15 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
- K040295: Applied Laparoscopic Monopolar Scissors (2004), 13 descendants of its own
- K063485: Logic Laparoscopic Scissors (2006), 7 descendants of its own
- K090583: Endoscopic Monopolar Scissors, Models Ems-235, Ems-165 (2009), 4 descendants of its own
- K062169: Applied Laparoscopic Disposable Monopolar Scissors (2006), 4 descendants of its own
- K141058: Ensizor Endoscopic Scissors (2014), 3 descendants of its own

Source page: https://510kreport.com/device/K903206
Methodology: https://510kreport.com/methodology