Clearance Summary
ZOLL M SERIES WITH RECTILINEAR BI-PHASIC OPTION (M SERIES BI-PHASIC) received FDA 510(k) clearance under submission number K032439, sponsored by Zoll Medical Corp. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-11-05.
- Submission: K032439
- Applicant / Sponsor: Zoll Medical Corp
- Clearance pathway: Abbreviated
- Review panel: Cardiovascular
- Device class: Class III
- Regulation citation: 21 CFR 870.5310
- Decision date: 2003-11-05
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.