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FDA 510(k) Application Details - K031195
Device Classification Name
Blood Pressure Cuff
More FDA Info for this Device
510(K) Number
K031195
Device Name
Blood Pressure Cuff
Applicant
ETHOX CORP.
P.O. BOX 7007
DEERFIELD, IL 60015 US
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Contact
DANIEL KAMM
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Regulation Number
870.1120
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Classification Product Code
DXQ
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More FDA Info for this Product Code
Date Received
04/16/2003
Decision Date
10/10/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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