FDA 510(k) Application Details - K991497

Device Classification Name Nystagmograph

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510(K) Number K991497
Device Name Nystagmograph
Applicant ICS MEDICAL CORP.
2227 HAMMOND DR.
SCHAUMBURG, IL 60173-3860 US
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Contact DELMAR F BLOEM
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Regulation Number 882.1460

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Classification Product Code GWN
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Date Received 04/29/1999
Decision Date 07/28/1999
Decision SESE - SUBST EQUIV
Classification Advisory Committee NE - Neurology
Review Advisory Committee NE - Neurology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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