HEG — Set, Anesthesia, Pudendal Class II

FDA Device Classification

FDA product code HEG covers "Set, Anesthesia, Pudendal", a Class II medical device regulated under 21 CFR 884.5100. Submissions are reviewed by the Obstetrics/Gynecology panel.

Classification Details

Product Code
HEG
Device Class
Class II
Regulation Number
884.5100
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No