Clearance Summary
MOTIVA MONITOR DEVICE CONNECTIVITY, MODEL# 453564036921 received FDA 510(k) clearance under submission number K071564, sponsored by Philips Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2007-08-31.
- Submission: K071564
- Applicant / Sponsor: Philips Medical Systems
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2910
- Decision date: 2007-08-31
Classification & Regulation
This clearance is catalogued under FDA product code DRG and 21 CFR 870.2910, within the Cardiovascular review panel as a Class II device.