K240992
- 510(k) number
- K240992
- Device name
- eMVFit (MVF-10M)
- Applicant
- Weero Co., Ltd. KR
- Product code
- IPF — Stimulator, Muscle, Powered
- Decision date
- 2024-10-10
- Date received
- 2024-04-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
510(k) Summary (official FDA PDF): K240992.pdf
Official FDA record: K240992
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.