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KXQ — Vibrator For Therapeutic Use, Genital Class II

FDA Device Classification

Classification Details

Product Code
KXQ
Device Class
Class II
Regulation Number
884.5960
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K142304reflexonicViberect Penile Vibratory Stimulation DeviceOctober 3, 2014
K110566reflexonicVIBERECT PENILE VIBRATORY STIMULATION DEVICEJune 24, 2011
K010096multiceptMULTI CARE THERAPEUTIC VIBRATORMarch 5, 2001
K955589multicept, apsFERTICARE PERSONAL THERAPEUTIC VIBRATORApril 11, 1996