Clearance Summary
Pelvic Floor Muscle Stimulator received FDA 510(k) clearance under submission number K230767, sponsored by Nanjing Vishee Medical Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2023-09-21.
- Submission: K230767
- Applicant / Sponsor: Nanjing Vishee Medical Technology Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5320
- Decision date: 2023-09-21
Classification & Regulation
This clearance is catalogued under FDA product code KPI and 21 CFR 876.5320, within the Gastroenterology, Urology review panel as a Class II device.