Clearance Summary
CARDIOPHONICS 1000 MEMORY MONITOR received FDA 510(k) clearance under submission number K992772, sponsored by Rlt Medical Assoc., Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1999-09-17.
- Submission: K992772
- Applicant / Sponsor: Rlt Medical Assoc., Inc.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2920
- Decision date: 1999-09-17
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.