Clearance Summary
MPC (MODEL 7000) EXTERNAL TEMPORARY PACEMAKER SYSTEM received FDA 510(k) clearance under submission number K970347, sponsored by Paladin Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1997-08-29.
- Submission: K970347
- Applicant / Sponsor: Paladin Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3600
- Decision date: 1997-08-29
Classification & Regulation
This clearance is catalogued under FDA product code DTE and 21 CFR 870.3600, within the Cardiovascular review panel as a Class II device.