HFK — Mold, Vaginal Class II

FDA Device Classification

FDA product code HFK covers "Mold, Vaginal", a Class II medical device regulated under 21 CFR 884.3900. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
HFK
Device Class
Class II
Regulation Number
884.3900
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K920838medsurg industriesMEDSURG CIRCUMCISION TRAYOctober 15, 1993