Clearance Summary
CENTRIMED SYSTEM 1 W/SYSTEM 1 ADAPTER received FDA 510(k) clearance under submission number K851613, sponsored by Centrimed Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1985-06-19.
- Submission: K851613
- Applicant / Sponsor: Centrimed Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4360
- Decision date: 1985-06-19
Classification & Regulation
This clearance is catalogued under FDA product code KFM and 21 CFR 870.4360, within the Cardiovascular review panel as a Class II device.