510(k) K143670
K143670 is an FDA 510(k) premarket notification submitted by Gn Otometrics A/S for the device "ICS CHARTR EP 200 WITH VEMP". The FDA issued a decision of Substantially Equivalent on October 23, 2015. The device falls under product code GWJ (Stimulator, Auditory, Evoked Response), a Class II device regulated under 21 CFR 882.1900. Gn Otometrics A/S has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 23, 2015
- Date Received
- December 24, 2014
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Auditory, Evoked Response
- Device Class
- Class II
- Regulation Number
- 882.1900
- Review Panel
- NE
- Submission Type