Clearance Summary
MEDILOG 6000-FD REPORT GENERATOR received FDA 510(k) clearance under submission number K890330, sponsored by Oxford Medilog, 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 1989-04-20.
- Submission: K890330
- Applicant / Sponsor: Oxford Medilog, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 1989-04-20
Classification & Regulation
This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.