KXQ — Vibrator For Therapeutic Use, Genital Class II
FDA product code KXQ covers "Vibrator For Therapeutic Use, Genital", a Class II medical device regulated under 21 CFR 884.5960. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 4 recent 510(k) clearances have been granted under this product code.
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-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K142304 | reflexonic | Viberect Penile Vibratory Stimulation Device | October 3, 2014 |
| K110566 | reflexonic | VIBERECT PENILE VIBRATORY STIMULATION DEVICE | June 24, 2011 |
| K010096 | multicept | MULTI CARE THERAPEUTIC VIBRATOR | March 5, 2001 |
| K955589 | multicept, aps | FERTICARE PERSONAL THERAPEUTIC VIBRATOR | April 11, 1996 |