FDA 510(k) Application Details - K950154

Device Classification Name Endoscope, Neurological

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510(K) Number K950154
Device Name Endoscope, Neurological
Applicant NEURO NAVIGATIONAL CORP.
3180 PULLMAN ST.
COSTA MESA, CA US
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Contact KAREN U SALINAS
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Regulation Number 882.1480

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Classification Product Code GWG
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Date Received 01/17/1995
Decision Date 07/14/1995
Decision SE - Substantially Equivalent
Classification Advisory Committee NE - Neurology
Review Advisory Committee NE - Neurology
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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