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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name device, monitoring, intracranial pressure
510(k) Number K914735
Device Name VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM
Applicant
CAMINO LABORATORIES, INC.
5955 PACIFIC CENTER BLVD.
SAN DIEGO,  CA  92121
Applicant Contact MARIE AKER
Correspondent
CAMINO LABORATORIES, INC.
5955 PACIFIC CENTER BLVD.
SAN DIEGO,  CA  92121
Correspondent Contact MARIE AKER
Regulation Number882.1620
Classification Product Code
GWM  
Date Received10/21/1991
Decision Date 01/17/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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