Clearance Summary
FEP-RINGED GORE-TEX@ VASCULAR GRAFT received FDA 510(k) clearance under submission number K821826, sponsored by W. L. Gore & Associates, 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 1982-12-29.
- Submission: K821826
- Applicant / Sponsor: W. L. Gore & Associates, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3450
- Decision date: 1982-12-29
Classification & Regulation
This clearance is catalogued under FDA product code DYF and 21 CFR 870.3450, within the Cardiovascular review panel as a Class II device.