# K910831: Endopath Surgical Instruments

- Pathway: 510(k) (Traditional)
- Applicant: Symbiosis Corp.
- Decided: May 31, 1991 after 93 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.
39 later devices descend from it; 1 cites it directly.
0 of 40 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
- K984240: Endopath Endoscopic Instruments (1999), 38 descendants of its own
- K061425: Purewrist Scissors, Model PW1101-01;Purewrist Dissector,  Model PW1201-01;Purewrist Hook, Model PW1301-01 (2006), 14 descendants of its own
- K173919: HX Device (2018), 8 descendants of its own
- K061417: Genicon Disposable Electrosurgical Instrumentation, Model 533-005-910 (2006), 6 descendants of its own
- K043541: Endolink True Movement System (2005), 4 descendants of its own

Source page: https://510kreport.com/device/K910831
Methodology: https://510kreport.com/methodology