HGG — Controller, Abortion Unit, Vacuum Class II

FDA Device Classification

FDA product code HGG covers "Controller, Abortion Unit, Vacuum", a Class II medical device regulated under 21 CFR 884.5070. 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
HGG
Device Class
Class II
Regulation Number
884.5070
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K883283galenica enterprisesDISPOSABLE AMNIOTOMEOctober 18, 1988