Clearance Summary
MAESTRO(R) MODELS 115, 118, 215 AND 218 PACEMAKERS received FDA 510(k) clearance under submission number K880326, sponsored by Cardiac Control Systems, 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 1988-04-11.
- Submission: K880326
- Applicant / Sponsor: Cardiac Control Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class III
- Regulation citation: 21 CFR 870.3610
- Decision date: 1988-04-11
Classification & Regulation
This clearance is catalogued under FDA product code DXY and 21 CFR 870.3610, within the Cardiovascular review panel as a Class III device.