Clearance Summary
CARDIOBEEPER(R) III received FDA 510(k) clearance under submission number K880300, sponsored by Survival Technology, 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 1988-05-12.
- Submission: K880300
- Applicant / Sponsor: Survival Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2920
- Decision date: 1988-05-12
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.