# K892895: Model 8800 Bipolar Coagulation Therapeutic System

- Pathway: 510(k) (Traditional)
- Applicant: Everest Medical Corp.
- Decided: Sep 25, 1989 after 153 days
- Product code: KNS (Unit, Electrosurgical, Endoscopic (With Or Without Accessories))
- Device class: 2
- Regulation: 21 CFR 876.4300
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K092571: Gyrus Acmi Biocoag Probe (2010), 2 descendants of its own
- K123319: Gyrus Acmi Bicoag Hemostasis Probe (2012), 1 descendant of its own
- K232633: Gold Probe Bipolar Electrohemostasis Catheter; Injection Gold Probe Bipolar Electrohemostasis Catheter (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K892895
Methodology: https://510kreport.com/methodology