Clearance Summary
CARDIOBEEPER CB250 received FDA 510(k) clearance under submission number K983582, sponsored by Merdian Medical Technologies , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1998-11-13.
- Submission: K983582
- Applicant / Sponsor: Merdian Medical Technologies , Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2920
- Decision date: 1998-11-13
Classification & Regulation
This clearance is catalogued under FDA product code DXH and 21 CFR 870.2920, within the Cardiovascular review panel as a Class II device.