MEQ — System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy Class III

FDA Device Classification

FDA product code MEQ covers "System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy", a Class III medical device. Submissions are reviewed by the Unknown panel.

Classification Details

Product Code
MEQ
Device Class
Class III
Regulation Number
Submission Type
Review Panel
GU
Medical Specialty
Unknown
Implant
No