Clearance Summary
DEEPVESSEL FFR received FDA 510(k) clearance under submission number K213657, sponsored by Keyamed Na, 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 2022-04-01.
- Submission: K213657
- Applicant / Sponsor: Keyamed Na, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1415
- Decision date: 2022-04-01
Classification & Regulation
This clearance is catalogued under FDA product code PJA and 21 CFR 870.1415, within the Cardiovascular review panel as a Class II device.