# K213247: JETT PLASMA Medical II

- Pathway: 510(k) (Traditional)
- Applicant: Compex, Spol, S.R.O.
- Decided: Mar 14, 2023 after 530 days
- Product code: QVJ (Low Power Electrosurgical Devices For Skin Lesion Destruction)
- 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
JETT PLASMA Medical II is used in the removal and destruction of skin lesions and coagulation of tissue.

Source page: https://510kreport.com/device/K213247
Methodology: https://510kreport.com/methodology