# K925984: Acucise Electrosurgical Trocar

- Pathway: 510(k) (Traditional)
- Applicant: Applied Medical Resources
- Decided: Jun 17, 1993 after 204 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; 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K012004: Easy Guide Electrosurgical Access Device (2001), 2 descendants of its own
- K013641: Senorx Biopsy Device, Driver, Control Module, Including Accessories (Power Cord,Connector Cords and Footswitch), Vacuums (2002), 1 descendant of its own
- K021707: Single Step Biopsy Device, Single Step Surgical Handle, Single Step Driver, Single Step Holders (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K925984
Methodology: https://510kreport.com/methodology