# K040763: Resect Medical Inline BI-Polar RF Linear Coagulation Device

- Pathway: 510(k) (Traditional)
- Applicant: Resect Medical, Inc.
- Decided: Apr 8, 2004 after 14 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
Longest line of descent: 1 generation back to K984552 (1999). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K984552: Cool-Tip RF System, Radionics, Inc. (1999) Summary page 2.

## Indications for use
The InLine MT Bi-Polar RF Linear Coagulation Device is intended to coagulate tissue during laparoscopic and intraoperative surgical procedures.

Source page: https://510kreport.com/device/K040763
Methodology: https://510kreport.com/methodology