Clearance Summary
Curapuls 670 received FDA 510(k) clearance under submission number K243112, sponsored by Enraf-Nonius, B.V.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2025-06-25.
- Submission: K243112
- Applicant / Sponsor: Enraf-Nonius, B.V.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5290
- Decision date: 2025-06-25
Classification & Regulation
This clearance is catalogued under FDA product code IMJ and 21 CFR 890.5290, within the Physical Medicine review panel as a Class II device.