Clearance Summary
VEIN GRAFT CANNULA received FDA 510(k) clearance under submission number K791832, sponsored by D/P, 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 1979-10-04.
- Submission: K791832
- Applicant / Sponsor: D/P, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4210
- Decision date: 1979-10-04
Classification & Regulation
This clearance is catalogued under FDA product code DWF and 21 CFR 870.4210, within the Cardiovascular review panel as a Class II device.