# K200372: Smoke Evacuation Fingerswitch, Smoke evacuation system with electrosurgical pencil

- Pathway: 510(k) (Traditional)
- Applicant: Modern Medical Equipment Manufacturing, Ltd.
- Decided: Nov 30, 2020 after 290 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: 2 generations back to K936304 (1994). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K103375: Plumepen Integrated Smoke Evacuation Pencil, Medtek Devices, Inc. (2011) Summary page 4.

## Most influential descendants
- K210315: Single Use Hand Switch Monopolar Forceps with Smoke Evacuation, Single Use Hand Switch Bipolar Forceps with Smoke Evacuation, Single Use Hand Switch Monopolar Forceps, Single Use Hand Switch Bipolar Forceps (2022), 0 descendants of its own

## Indications for use
The device is used to conduct electrosurgical current from an electrosurgical generator to target tissue in electrosurgical procedures for monopolar cutting and coagulation, with the additional function of evacuation to facilitate the removal of surgical smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system.

Source page: https://510kreport.com/device/K200372
Methodology: https://510kreport.com/methodology