Clearance Summary
MODEL 5866-9M & MODEL 6981M received FDA 510(k) clearance under submission number K911827, sponsored by Metronic, 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 1991-07-23.
- Submission: K911827
- Applicant / Sponsor: Metronic, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3620
- Decision date: 1991-07-23
Classification & Regulation
This clearance is catalogued under FDA product code DTD and 21 CFR 870.3620, within the Cardiovascular review panel as a Class II device.