Clearance Summary
SHERPA GUIDING CATHETER WITH CATHETER INTRODUCER received FDA 510(k) clearance under submission number K915351, sponsored by Medtronics Interventional Vascular. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1992-06-29.
- Submission: K915351
- Applicant / Sponsor: Medtronics Interventional Vascular
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1200
- Decision date: 1992-06-29
Classification & Regulation
This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.