Clearance Summary
CAREFUSION NICOLET EDX received FDA 510(k) clearance under submission number K120979, sponsored by Carefusion 209, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2012-04-25.
- Submission: K120979
- Applicant / Sponsor: Carefusion 209, Inc.
- Clearance pathway: Special
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1870
- Decision date: 2012-04-25
Classification & Regulation
This clearance is catalogued under FDA product code GWF and 21 CFR 882.1870, within the Neurology review panel as a Class II device.