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

Stimulator, Autonomic Nerve, Implanted For Epilepsy

Unknown
FDA source (opens on fda.gov)

LYJ is the FDA product code for Stimulator, Autonomic Nerve, Implanted For Epilepsy, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 37 recalls.

Classification record

Product code
LYJ
Device name
Stimulator, Autonomic Nerve, Implanted For Epilepsy
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
37

Companies listing this code with FDA

Companies whose registered establishments list this code