Clearance Summary
Reprocessed Reflexion Spiral Bi-Directional Variable Radius Electrophysiology Catheter received FDA 510(k) clearance under submission number K191170, sponsored by Innovative Health, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2019-10-30.
- Submission: K191170
- Applicant / Sponsor: Innovative Health, LLC
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1220
- Decision date: 2019-10-30
Classification & Regulation
This clearance is catalogued under FDA product code NLH and 21 CFR 870.1220, within the Cardiovascular review panel as a Class II device.