Clearance Summary
MASTRO PLUS BALLOON IN-DEFLATION DEVICE received FDA 510(k) clearance under submission number K140943, sponsored by Beijing Demax Medical Technology Co.,Ltd. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2015-03-05.
- Submission: K140943
- Applicant / Sponsor: Beijing Demax Medical Technology Co.,Ltd
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1650
- Decision date: 2015-03-05
Classification & Regulation
This clearance is catalogued under FDA product code MAV and 21 CFR 870.1650, within the Cardiovascular review panel as a Class II device.