Product code KXQ— Obstetrics/Gynecology
FERTICARE PERSONAL THERAPEUTIC VIBRATOR
- Classification name
- Vibrator For Therapeutic Use, Genital
- Device class
- Class 2
- Regulation
- 21 CFR 884.5960
- Advisory panel
- Obstetrics/Gynecology
- Total cleared
- 4
- First cleared
- Most recent
Market context for product code KXQ
FDA has cleared devices under product code KXQ between 1996 and 2014, filed by 3 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2014
- 2011
- 2001
- 1996
Top applicants under product code KXQ
Recent clearances under product code KXQ
Data sourced from openFDA. This site is unofficial and independent of the FDA.