Clearance Summary
Angel Catheter received FDA 510(k) clearance under submission number K160747, sponsored by Bio2 Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2016-07-28.
- Submission: K160747
- Applicant / Sponsor: Bio2 Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3375
- Decision date: 2016-07-28
Classification & Regulation
This clearance is catalogued under FDA product code PNS and 21 CFR 870.3375, within the Cardiovascular review panel as a Class II device.