510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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GXCClass III

Device, Electroconvulsive Therapy

21 CFR 882.5940 / Neurology
FDA source (opens on fda.gov)

GXC is the FDA product code for Device, Electroconvulsive Therapy, a class III device type, regulated under 21 CFR 882.5940. As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
GXC
Device name
Device, Electroconvulsive Therapy
Regulation
21 CFR 882.5940
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
0

Companies listing this code with FDA

Companies whose registered establishments list this code