Clearance Summary
ARCOLITH 2100-CARDIAC PULSE GENERATOR received FDA 510(k) clearance under submission number K792216, sponsored by Arco Medical Products Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1979-11-29.
- Submission: K792216
- Applicant / Sponsor: Arco Medical Products Co.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class III
- Regulation citation: 21 CFR 870.3610
- Decision date: 1979-11-29
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.