K243112
- 510(k) number
- K243112
- Device name
- Curapuls 670
- Applicant
- Enraf-Nonius, B.V. NL
- Product code
- IMJ — Diathermy, Shortwave, For Use In Applying Therapeuti
- Decision date
- 2025-06-25
- Date received
- 2024-09-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K243112.pdf
Official FDA record: K243112
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.