HGH — Cannula, Suction, Uterine Class II

FDA Device Classification

FDA product code HGH covers "Cannula, Suction, Uterine", a Class II medical device regulated under 21 CFR 884.5070. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 6 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
HGH
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
K172151chongquin jinshan science and technology (group) coHysteroscopy SystemApril 9, 2018
K161106panpac medical corporationPANPAC DISPOSABLE VACUUM CURETTESJanuary 13, 2017
K140213dongguan microview medical technology coDISPOSABLE ENDOSCOPIC CANNULAMarch 25, 2015
K093508womancare globalRIGID CANNULAE CURVED (RC6-RC12), RIGID CANNULAE STRAIGHT (RS6-RS12)March 4, 2010
K935820kolster methodsKOLSTER METHODSJuly 19, 1994
K840285imex medical systemsNON STRESS TEST MONITOR 507May 9, 1984