JXKClass III

Cranial Electrotherapy Stimulator To Treat Depression

21 CFR 882.5800 / Neurology

JXK is the FDA product code for Cranial Electrotherapy Stimulator To Treat Depression, a class III device type, regulated under 21 CFR 882.5800. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and 3 recalls.

Classification record

Product code: JXK
Device name: Cranial Electrotherapy Stimulator To Treat Depression
Regulation: 21 CFR 882.5800
Device class: Class III
Review panel: Neurology
Submission type: PMA
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 3

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code JXK

FDA records hold no clearances under product code JXK.

Recent recalls

Product code JXK

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)