# K132300: Epix Electrosurgical Probe Spatula Tip, Epix Electrosurgical Probe L-Hook Tip, Epix Electrosurgical Probe J-Hook Tip, RE

- Pathway: 510(k) (Traditional)
- Applicant: Applied Medical Resources Corp.
- Decided: Jan 24, 2014 after 184 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 K983623 (1998). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K983623: Modulap, Atc Technologies, Inc. (1998) Summary page 1.

## Most influential descendants
- K171684: Epix Electrosurgical Probe with Smoke Evacuation (2017), 0 descendants of its own

## Indications for use
The Epixo Electrosurgical Probes are indicated for irrigation, evacuation of fluids, and electrosurgical cutting and coagulation during general laparoscopic procedures.

Source page: https://510kreport.com/device/K132300
Methodology: https://510kreport.com/methodology