Clearance Summary
ZOLL E SERIES WITH 2010 AHA GUIDLINES SOFTWARE UPDATE received FDA 510(k) clearance under submission number K110168, sponsored by Zoll Medical Corporation, World Wide Headquarters. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-02-17.
- Submission: K110168
- Applicant / Sponsor: Zoll Medical Corporation, World Wide Headquarters
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class III
- Regulation citation: 21 CFR 870.5310
- Decision date: 2011-02-17
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.