# K161134: Bovie Bantam/PRO Electrosurgical Generator, Bovie DERM 941 Electrosurgical Generator, Bovie DERM 942 Electrosurgical Generator

- Pathway: 510(k) (Traditional)
- Applicant: Bovie Medical Corporation
- Decided: Jun 20, 2016 after 59 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: 5 generations back to K933002 (1994). 13 ancestors in all.
14 later devices descend from it; 2 cite it directly.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K021817: Aaron A950 High Frequency Electrosurgical Generator, Aaron A950 Electrosurgical Generator, 240V, Aaron Medical Industries (2002) Summary page 5.
- K000961: Aaron 900 High Frequency Dessiccator/Handpiece, Aaron Medical Industries (2000) Summary page 5.
- K134054: Bovie Ids-310 High Frequency Electrosurgical Generator, Aaron A3350 High Frequency Electrosurgical Generator, Bovie Medical Corporation (2014) Summary page 5.

## Most influential descendants
- K192813: Plasma IQ (2020), 12 descendants of its own
- K212329: Plasma IQ (2021), 5 descendants of its own
- K201738: SubNovii Advanced Plasma Technology (2020), 5 descendants of its own
- K223222: Plasma IQ (2023), 3 descendants of its own
- K241099: Plasonic (Plasonic) (2024), 2 descendants of its own

## Indications for use
The intended use for the DERM 941 and DERM 942 is for removal and destruction of skin lesions and the coagulation of tissue. The intended use for the Bantam/PRO is for removal and destruction of skin lesions and for electrosurgical cutting, blending, coagulation, fulguration, and bipolar procedures.

Source page: https://510kreport.com/device/K161134
Methodology: https://510kreport.com/methodology