Clearance Summary
REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM received FDA 510(k) clearance under submission number K102418, sponsored by Reverse Medical Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-04-15.
- Submission: K102418
- Applicant / Sponsor: Reverse Medical Corporation
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 2011-04-15
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.