510(k) K152505
K152505 is an FDA 510(k) premarket notification submitted by Inomed Medizintechnik GmbH for the device "C2 NerveMonitor System". The FDA issued a decision of Substantially Equivalent on February 1, 2016. The device falls under product code ETN (Stimulator, Nerve), a Class II device regulated under 21 CFR 874.1820. Inomed Medizintechnik GmbH has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 1, 2016
- Date Received
- September 2, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Nerve
- Device Class
- Class II
- Regulation Number
- 874.1820
- Review Panel
- EN
- Submission Type