Clearance Summary
PHILIPS ECG LEADWIRE SET received FDA 510(k) clearance under submission number K110287, sponsored by Philips Medical Systems. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-02-15.
- Submission: K110287
- Applicant / Sponsor: Philips Medical Systems
- Clearance pathway: Abbreviated
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2900
- Decision date: 2011-02-15
Classification & Regulation
This clearance is catalogued under FDA product code DSA and 21 CFR 870.2900, within the Cardiovascular review panel as a Class II device.