Clearance Summary
PRECLUDE IMA SLEEVE received FDA 510(k) clearance under submission number K960532, 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 1996-05-23.
- Submission: K960532
- Applicant / Sponsor: W. L. Gore & Associates, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3470
- Decision date: 1996-05-23
Classification & Regulation
This clearance is catalogued under FDA product code MFX and 21 CFR 870.3470, within the Cardiovascular review panel as a Class II device.