# K934784: Endopath Endoscopic Electrosurgical Forceps with Cutting Feature

- Pathway: 510(k) (Traditional)
- Applicant: ETHICON, Inc.
- Decided: Mar 4, 1994 after 150 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- 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; 2 cite 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
- K012625: Reprocessed Unipolar Laparoscopic/Endoscopic Instruments (2001), 2 descendants of its own
- K240334: LAGIS Endoscopic Instruments - Grasper (DI-5670-33D, DI-5670-45D, DI-5716-33D, DI-5716-45D, DI-5719-33D,  DI-5731-33D, DI-5731-45D,  DI-5901-33D, DI-5901-45D) (2024), 0 descendants of its own
- K031869: Siss Inc. (D.B.a. Medisiss) Reprocessed Electrosurgical Instruments and Accessories (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K934784
Methodology: https://510kreport.com/methodology