# Vibrator For Therapeutic Use, Genital
> **Product code: KXQ** · Class II — Moderate Risk (510(k) clearance required) · Obstetrics/Gynecology · 21 CFR 884.5960
## Classification
- **FDA Product Code:** KXQ
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 884.5960
- **Review panel:** OB
- **Medical specialty:** Obstetrics/Gynecology
- **Submission type:** 4
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** N
## Market data
- **Cleared 510(k) submissions:** 4
- **Registered establishments:** 34
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=KXQ)
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