FHG — Bell, Circumcision Class II

FDA Device Classification

FDA product code FHG covers "Bell, Circumcision", a Class II medical device regulated under 21 CFR 884.4530. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K911272edward weckENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705July 2, 1991
K770873american hospital supplyCIRCUMCISION KITJuly 11, 1977