Home / Device Classification / HHG

HHG — Dilator, Cervical, Vibratory Class III

FDA Device Classification

FDA product code HHG covers "Dilator, Cervical, Vibratory", a Class III medical device regulated under 21 CFR 884.4270. Submissions are reviewed by the Obstetrics/Gynecology panel.

Classification Details

Product Code: HHG
Device Class: Class III
Regulation Number: 884.4270
Submission Type
Review Panel: OB
Medical Specialty: Obstetrics/Gynecology
Implant: No

Definition

Call for PMAs to be filed by 12/26/96 per 61 FR 50708 on 9/27/96