Clearance Summary
CARDIOBEEPER CB-12L received FDA 510(k) clearance under submission number K965101, sponsored by Meridian Medical Technologies, 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 1997-03-17.
- Submission: K965101
- Applicant / Sponsor: Meridian Medical Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2920
- Decision date: 1997-03-17
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.