Clearance Summary
PANTRIDGE MK III DEFIBRILLATOR/MONITOR received FDA 510(k) clearance under submission number K780416, sponsored by Ipco Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1978-04-21.
- Submission: K780416
- Applicant / Sponsor: Ipco Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5300
- Decision date: 1978-04-21
Classification & Regulation
This clearance is catalogued under FDA product code LDD and 21 CFR 870.5300, within the Cardiovascular review panel as a Class II device.