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510(k) K111647

C2 NERVEMONITOR SYSTEM WITH ACCESSORIES by Inomed Medizintechnik GmbH — Product Code GWF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 6, 2011
Date Received
June 13, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stimulator, Electrical, Evoked Response
Device Class
Class II
Regulation Number
882.1870
Review Panel
NE
Submission Type

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