# K223222: Plasma IQ

- Pathway: 510(k) (Special)
- Applicant: Neauvia North America, Inc.
- Decided: Jan 17, 2023 after 92 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: 8 generations back to K933002 (1994). 16 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K212329: Plasma IQ, Neauvia North America, Inc. (2021) Summary page 4.

## Most influential descendants
- K241099: Plasonic (Plasonic) (2024), 2 descendants of its own
- K260397: SYNERJET PRO (SP-1002); InPhiuse (SP-1002); WOWJET (SP-1002) (2026), 0 descendants of its own
- K251334: New Doublo 2.0 (2025), 0 descendants 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/K223222
Methodology: https://510kreport.com/methodology