# K092732: Propencil Esu Pencil

- Pathway: 510(k) (Traditional)
- Applicant: Bio Protech, Inc.
- Decided: Nov 25, 2009 after 82 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 K896626 (1990). 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)
- K896626: Hand Controlled Electrosurgical Pencils, Conmedcorp (1990) Summary page 1.

## Most influential descendants
- K232407: Cautery Protective Actuation System (CPAS) (2023), 0 descendants of its own

## Indications for use
The PROPENCIL ESU Pencil is intended for use in general surgical procedures to deliver electrosurgical energy to the surgery site for tissue cutting and coagulation.

Source page: https://510kreport.com/device/K092732
Methodology: https://510kreport.com/methodology