Clearance Summary
SCORPION Portal Vein Access Set received FDA 510(k) clearance under submission number K213002, sponsored by Argon Medical Devices. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2021-10-14.
- Submission: K213002
- Applicant / Sponsor: Argon Medical Devices
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1340
- Decision date: 2021-10-14
Classification & Regulation
This clearance is catalogued under FDA product code DYB and 21 CFR 870.1340, within the Cardiovascular review panel as a Class II device.