Clearance Summary
PRO-GUIDE received FDA 510(k) clearance under submission number K911747, sponsored by American Interventional Technology. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1991-09-18.
- Submission: K911747
- Applicant / Sponsor: American Interventional Technology
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 1991-09-18
Classification & Regulation
This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.