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HGF — Source, Abortion Unit, Vacuum Class II

FDA Device Classification

Classification Details

Product Code
HGF
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
K945179medgyn productsBOTTLE COLLECTION SETJanuary 26, 1995
K905115douglas james donaldson compliance servicesBIOVISION ENDOCULAR PROBEFebruary 11, 1991
K904248charles l. rose and coMODEL GLASE 210 HOLMIUM LASER SYSTEMDecember 14, 1990
K890787hgm medical laser systemsO-020 LASER INDIRECT OPHTHALMOSCOPEMarch 24, 1989