FDA 510(k) Applications for Medical Device Product Code "KXQ"
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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 |