MOH — Monitor, Heart Rate, Fetal, Non-Stress Test (Home Use) Class II

FDA Device Classification

FDA product code MOH covers "Monitor, Heart Rate, Fetal, Non-Stress Test (Home Use)", a Class II medical device regulated under 21 CFR 884.2730. Submissions are reviewed by the Obstetrics/Gynecology panel.

Classification Details

Product Code
MOH
Device Class
Class II
Regulation Number
884.2730
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No