HEZ — Endoscope, Transcervical (Amnioscope)(And Accessories) Class II

FDA Device Classification

FDA product code HEZ covers "Endoscope, Transcervical (Amnioscope)(And Accessories)", a Class II medical device regulated under 21 CFR 884.1660. Submissions are reviewed by the Obstetrics/Gynecology panel.

Classification Details

Product Code
HEZ
Device Class
Class II
Regulation Number
884.1660
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No