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FDA 510(k) Application Details - K982702
Device Classification Name
Device, Monitoring, Intracranial Pressure
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510(K) Number
K982702
Device Name
Device, Monitoring, Intracranial Pressure
Applicant
CAMINO NEUROCARE, INC.
5955 PACIFIC CENTER BLVD.
SAN DIEGO, CA 92121 US
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Contact
JODY J FLEMING
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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
08/03/1998
Decision Date
09/10/1998
Decision
SESE - SUBST EQUIV
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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