Clearance Summary
POWERHEART G5 AED received FDA 510(k) clearance under submission number K122758, sponsored by Cardiac Science Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2014-02-12.
- Submission: K122758
- Applicant / Sponsor: Cardiac Science Corporation
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class III
- Regulation citation: 21 CFR 870.5310
- Decision date: 2014-02-12
Classification & Regulation
This clearance is catalogued under FDA product code MKJ and 21 CFR 870.5310, within the Cardiovascular review panel as a Class III device.