FDA Product Code
FDA Product Code KXQ — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Obstetrics/Gynecology
- 21 CFR Citation
- 884.5960
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K142304 | Viberect Penile Vibratory Stimulation Device | Reflexonic, LLC | 2014-10-03 | Traditional | PDF ↗ |
| K110566 | VIBERECT PENILE VIBRATORY STIMULATION DEVICE | Reflexonic, LLC | 2011-06-24 | Traditional | PDF ↗ |
| K010096 | MULTI CARE THERAPEUTIC VIBRATOR | Multicept A/S | 2001-03-05 | Special | PDF ↗ |
| K955589 | FERTICARE PERSONAL THERAPEUTIC VIBRATOR | Multicept, Aps. | 1996-04-11 | Traditional | PDF ↗ |
Product code KXQ · Class II · Obstetrics/Gynecology. Data: openFDA.