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

Stimulator, Electrical, Implanted, For Parkinsonian Tremor

Unknown
FDA source (opens on fda.gov)

MHY is the FDA product code for Stimulator, Electrical, Implanted, For Parkinsonian Tremor, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 46 recalls.

Classification record

Product code
MHY
Device name
Stimulator, Electrical, Implanted, For Parkinsonian Tremor
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
46

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 27 companies shown, in name order