Clearance Summary
LIFEPAK 20 DEFIBRILLATOR/ MONITOR received FDA 510(k) clearance under submission number K063119, sponsored by Medtronic Emergency Response Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-12-22.
- Submission: K063119
- Applicant / Sponsor: Medtronic Emergency Response Systems, Inc.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class III
- Regulation citation: 21 CFR 870.5310
- Decision date: 2006-12-22
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.