Clearance Summary
506CN PATIENT MONITOR received FDA 510(k) clearance under submission number K091050, sponsored by Criticare Systems, 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 2009-05-27.
- Submission: K091050
- Applicant / Sponsor: Criticare Systems, Inc.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2300
- Decision date: 2009-05-27
Classification & Regulation
This clearance is catalogued under FDA product code DRT and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.