Pelvic Floor Stimulator (Intrelief PFE)— 510(k) K241899
Substantially EquivalentEasymed Instruments Co., Ltd.
FDA 510(k) clearance K241899 for Pelvic Floor Stimulator (Intrelief PFE), Substantially Equivalent on 2024-11-27. Applicant: Easymed Instruments Co., Ltd..
Clearance details
- Applicant
- Easymed Instruments Co., Ltd.
- Product code
- Code KPI
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Foshan, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.