# K992186: Quad Bipolar Laparoscopic Coagulating and Cutting Instrument

- Pathway: 510(k) (Traditional)
- Applicant: Conmedcorp
- Decided: Jul 30, 1999 after 31 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
For use in laparoscopic and open surgical procedures to provide mechanical cutting and electrosurgical hemostasis of tissue as well as grasping and manipulation of the tissue.

Source page: https://510kreport.com/device/K992186
Methodology: https://510kreport.com/methodology