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FDA 510(k) Application Details - K962928
Device Classification Name
Device, Monitoring, Intracranial Pressure
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510(K) Number
K962928
Device Name
Device, Monitoring, Intracranial Pressure
Applicant
CAMINO NEUROCARE, INC.
5955 PACIFIC CENTER BLVD.
SAN DIEGO, CA 92121 US
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DONNA L FREE
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Regulation Number
882.1620
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Classification Product Code
GWM
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More FDA Info for this Product Code
Date Received
07/29/1996
Decision Date
12/20/1996
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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