Clearance Summary
Needle's Eye Snare Retrieval Set - 54cm received FDA 510(k) clearance under submission number K163353, 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 2017-07-11.
- Submission: K163353
- Applicant / Sponsor: Cook Incorporated
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5150
- Decision date: 2017-07-11
Classification & Regulation
This clearance is catalogued under FDA product code DXE and 21 CFR 870.5150, within the Cardiovascular review panel as a Class II device.