FDA 510(k) Applications for Medical Device Product Code "KXQ"
(Vibrator For Therapeutic Use, Genital)

FDA 510(k) Number Applicant Device Name Decision Date
K010096 MULTICEPT A/S MULTI CARE THERAPEUTIC VIBRATOR 03/05/2001
K955589 MULTICEPT APS FERTICARE PERSONAL THERAPEUTIC VIBRATOR 04/11/1996
K110566 REFLEXONIC, LLC VIBERECT PENILE VIBRATORY STIMULATION DEVICE 06/24/2011
K142304 REFLEXONIC, LLC Viberect Penile Vibratory Stimulation Device 10/03/2014


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