Clearance Summary
M300 MONITOR/CONTROLLER T500 TREADMILL received FDA 510(k) clearance under submission number K873774, sponsored by Burdick Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1987-11-06.
- Submission: K873774
- Applicant / Sponsor: Burdick Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2450
- Decision date: 1987-11-06
Classification & Regulation
This clearance is catalogued under FDA product code DXJ and 21 CFR 870.2450, within the Cardiovascular review panel as a Class II device.