HDH — Needle, Cerclage, Gynecological Class I

FDA Device Classification

FDA product code HDH covers "Needle, Cerclage, Gynecological", a Class I medical device regulated under 21 CFR 884.4530. Submissions are reviewed by the Obstetrics/Gynecology panel.

Classification Details

Product Code
HDH
Device Class
Class I
Regulation Number
884.4530
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No