Clearance Summary
Advance 14LP Low Profile PTA Balloon Dilatation Catheter received FDA 510(k) clearance under submission number K170193, sponsored by Cook Incorporated. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2017-02-13.
- Submission: K170193
- Applicant / Sponsor: Cook Incorporated
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 2017-02-13
Classification & Regulation
This clearance is catalogued under FDA product code LIT and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.