Clearance Summary
Reprocessed Advisor HD Grid Mapping Catheter, Sensor Enabled received FDA 510(k) clearance under submission number K200212, 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 2020-09-03.
- Submission: K200212
- Applicant / Sponsor: Innovative Health, LLC
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1220
- Decision date: 2020-09-03
Classification & Regulation
This clearance is catalogued under FDA product code MTD and 21 CFR 870.1220, within the Cardiovascular review panel as a Class II device.