K232786
- 510(k) number
- K232786
- Device name
- Stimulation System (PA series, PR series, S series and Q series)
- Applicant
- Edan Instruments, Inc. CN
- Product code
- IPF — Stimulator, Muscle, Powered
- Decision date
- 2024-05-16
- Date received
- 2023-09-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K232786.pdf
Official FDA record: K232786
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.