MHZ — Stimulator, Vestibular Acceleration, Therapeutic Class III

FDA Device Classification

FDA product code MHZ covers "Stimulator, Vestibular Acceleration, Therapeutic", a Class III medical device. Submissions are reviewed by the Unknown panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K843355kontron instrumentsTRANSDUCER FOR KONTROL 5MHZ SIGMA 20December 3, 1984