Home / Device Classification / HGD

HGD — Applicator, Vaginal Class I

FDA Device Classification

Classification Details

Product Code: HGD
Device Class: Class I
Regulation Number: 884.4520
Submission Type
Review Panel: OB
Medical Specialty: Obstetrics/Gynecology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K823517	kline technologies	THE KLINE APPLICATOR	January 18, 1983