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

System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy

Unknown
FDA source (opens on fda.gov)

MEQ is the FDA product code for System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 9 recalls.

Classification record

Product code
MEQ
Device name
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
9

Companies listing this code with FDA

Companies whose registered establishments list this code