# K930666: Reusable Laparoscopic Instruments W/ Electrocautery

- Pathway: 510(k) (Traditional)
- Applicant: Snowden-Pencer
- Decided: May 19, 1994 after 464 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.
274 later devices descend from it; 1 cites it directly.
1 of 275 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K960400: Diamond-Touch and Micro Diamond-Touch Instruments/Diamond-Line Instruments/Diamond-Port (Access Parts) (1996), 273 descendants of its own
- K990144: Intuitive Surgical Endoscopic Instruments, Intuitive Surgical Endoscopic Instrument Control System (2000), 269 descendants of its own
- K022574: Intuitive Surgical Endoscopic Instrument Control System & Endoscopic Instruments, Model DA Vinci Isi 1000/1200 (2002), 260 descendants of its own
- K021036: Intuitive Surgical DA Vinci Surgical System, Model IS1000 (2002), 260 descendants of its own
- K040237: Intuitive Surgical DA Vinci Endoscopic Instrument Control System and Endoscopic Instruments (2004), 258 descendants of its own

Source page: https://510kreport.com/device/K930666
Methodology: https://510kreport.com/methodology