Clearance Summary
Viberect Penile Vibratory Stimulation Device received FDA 510(k) clearance under submission number K142304, sponsored by Reflexonic, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2014-10-03.
- Submission: K142304
- Applicant / Sponsor: Reflexonic, LLC
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5960
- Decision date: 2014-10-03
Classification & Regulation
This clearance is catalogued under FDA product code KXQ and 21 CFR 884.5960, within the Obstetrics/Gynecology review panel as a Class II device.