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HHF — Remover, Intrauterine Device, Contraceptive, Hook-Type Class I

FDA Device Classification

Classification Details

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K926541thomasville medical assocIUD HOOKSFebruary 24, 1994
K891030zinnanti surgical instrumentsIUD HOOKS - SIMPLE, UNIVERSAL AND SKLARMarch 17, 1989
K842295premier dental productsINTRAUTERINE DEVICE REMOVEROctober 12, 1984
K831568f. and f. koenigkramerRELIANCE TEMPO OPHTH. INSTR STANDJune 30, 1983
K820115proto-medEMMETT IUD THREAD RETREIVERFebruary 5, 1982
K811761proto-medTHE EMMETT IUD THREAD RETRIEVERSeptember 21, 1981