Clearance Summary
CARDIOBEEPER CB12/12, MODEL CB12/12 received FDA 510(k) clearance under submission number K002310, sponsored by Meridian 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 2000-10-25.
- Submission: K002310
- Applicant / Sponsor: Meridian Medical Technologies , Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2920
- Decision date: 2000-10-25
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.