Clearance Summary
CG+ Arrow JACC received FDA 510(k) clearance under submission number K161765, sponsored by Arrow International, Inc. (Subsidiary of Teleflex. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2016-09-06.
- Submission: K161765
- Applicant / Sponsor: Arrow International, Inc. (Subsidiary of Teleflex
- Clearance pathway: Special
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5970
- Decision date: 2016-09-06
Classification & Regulation
This clearance is catalogued under FDA product code LJS and 21 CFR 880.5970, within the General Hospital review panel as a Class II device.