# K192813: Plasma IQ

- Pathway: 510(k) (Traditional)
- Applicant: Neauvia North America, Inc.
- Decided: Mar 6, 2020 after 157 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: 6 generations back to K933002 (1994). 14 ancestors in all.
12 later devices descend from it; 3 cite it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K161134: Bovie Bantam/PRO Electrosurgical Generator, Bovie DERM 941 Electrosurgical Generator, Bovie DERM 942 Electrosurgical Generator, Bovie Medical Corporation (2016) Summary page 4.

## Most influential descendants
- 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
- K233123: Silkro (2024), 1 descendant of its own

## Indications for use
Plasma IQ is used in the removal and destruction of skin lesions and coagulation of tissue.

Source page: https://510kreport.com/device/K192813
Methodology: https://510kreport.com/methodology