Clearance Summary
AC3 Series Intra-Aortic Balloon Pump (IABP) received FDA 510(k) clearance under submission number K192238, sponsored by Arrow International, Teleflex. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2019-11-12.
- Submission: K192238
- Applicant / Sponsor: Arrow International, Teleflex
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3535
- Decision date: 2019-11-12
Classification & Regulation
This clearance is catalogued under FDA product code DSP and 21 CFR 870.3535, within the Cardiovascular review panel as a Class II device.