Clearance Summary
PTI INTRA-ART INTERNAL MAMMARY ARTERY CANNULA KIT received FDA 510(k) clearance under submission number K894684, sponsored by Pioneering Technologies, 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 1989-10-17.
- Submission: K894684
- Applicant / Sponsor: Pioneering Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4210
- Decision date: 1989-10-17
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.