K232937
- 510(k) number
- K232937
- Device name
- BTL-899M
- Applicant
- BTL Industries, Inc. MA · US
- Product code
- IPF — Stimulator, Muscle, Powered
- Decision date
- 2023-12-26
- Date received
- 2023-09-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K232937.pdf
Official FDA record: K232937
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.