HEH — Chamber, Decompression, Abdominal Class III

FDA Device Classification

FDA product code HEH covers "Chamber, Decompression, Abdominal", a Class III medical device regulated under 21 CFR 884.5225. Submissions are reviewed by the Obstetrics/Gynecology panel.

Classification Details

Product Code
HEH
Device Class
Class III
Regulation Number
884.5225
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No