Clearance Summary
Small (4) Roller Pump for the Terumo Advanced Perfusion System 1, Large (6) Roller Pump for the Terumo Advanced Perfusion System 1 received FDA 510(k) clearance under submission number K162843, sponsored by Terumo Cardiovascular Systems Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2016-11-17.
- Submission: K162843
- Applicant / Sponsor: Terumo Cardiovascular Systems Corporation
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4370
- Decision date: 2016-11-17
Classification & Regulation
This clearance is catalogued under FDA product code DWB and 21 CFR 870.4370, within the Cardiovascular review panel as a Class II device.