# K945975: Evershears (R) Scissors, Bilap (R) Probes, Bicoag (R) Forceps

- Pathway: 510(k) (Traditional)
- Applicant: Everest Medical Corp.
- Decided: Dec 21, 1994 after 13 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.
186 later devices descend from it; 13 cite it directly.
5 of 187 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
- K011722: Atricure Bipolar Coagulation System (2001), 92 descendants of its own
- K020919: Atricure Bipolar System, Models ASU1, ASU2, ASU3, LHP1, LHP2, RHP1 (2002), 90 descendants of its own
- K030512: Guidant Vasoview Endoscopic Vessel Harvesting System (2003), 62 descendants of its own
- K060723: 40 L High Flow Insufflator F113 (2006), 45 descendants of its own
- K063367: 45L Core Insufflator, Model F114 (2007), 44 descendants of its own

Source page: https://510kreport.com/device/K945975
Methodology: https://510kreport.com/methodology