Clearance Summary
FluidiTube 2.7F Infusion Micro Catheter, 110 cm and 130 cm received FDA 510(k) clearance under submission number K161967, sponsored by Callisyn Biomedical, 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 2017-01-27.
- Submission: K161967
- Applicant / Sponsor: Callisyn Biomedical, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1210
- Decision date: 2017-01-27
Classification & Regulation
This clearance is catalogued under FDA product code KRA and 21 CFR 870.1210, within the Cardiovascular review panel as a Class II device.