# Stimulator, Vaginal, Muscle, Powered, For Therapeutic Use
> **Product code: HII** · Class III — High Risk (PMA approval required, life-sustaining) · Obstetrics/Gynecology · 21 CFR 884.5940
## Classification
- **FDA Product Code:** HII
- **Device class:** Class III — High Risk (PMA approval required, life-sustaining)
- **Regulation:** 21 CFR 884.5940
- **Review panel:** OB
- **Medical specialty:** Obstetrics/Gynecology
- **Submission type:** 2
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** N
## Definition

Call for PMAs to be filed by 7/12/2000 per 65 FR 19834 on 4/13/00

## Market data
- **Cleared 510(k) submissions:** 0
- **Registered establishments:** 0
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=HII)
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