Clearance Summary
CPRmeter 2 CPR Feedback Device received FDA 510(k) clearance under submission number K173886, sponsored by Laerdal Medical AS. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2018-03-23.
- Submission: K173886
- Applicant / Sponsor: Laerdal Medical AS
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5210
- Decision date: 2018-03-23
Classification & Regulation
This clearance is catalogued under FDA product code LIX and 21 CFR 870.5210, within the Cardiovascular review panel as a Class II device.