Clearance Summary
C2 NERVEMONITOR SYSTEM WITH ACCESSORIES received FDA 510(k) clearance under submission number K111647, sponsored by Inomed Medizintechnik GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2011-10-06.
- Submission: K111647
- Applicant / Sponsor: Inomed Medizintechnik GmbH
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1870
- Decision date: 2011-10-06
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.