K223802
- 510(k) number
- K223802
- Device name
- accufit
- Applicant
- Mettler Electronics Corporation CA · US
- Product code
- IPF — Stimulator, Muscle, Powered
- Decision date
- 2023-10-06
- Date received
- 2022-12-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 1.7 MB · U.S. public domain
Also available from FDA: K223802.pdf
Official FDA record: K223802
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.