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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 K881183
Device Name VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4H
Applicant
CAMINO LABORATORIES, INC.
5955 PACIFIC CENTER BLVD.
SAN DIEGO,  CA  92121
Applicant Contact DAN MCKAY
Correspondent
CAMINO LABORATORIES, INC.
5955 PACIFIC CENTER BLVD.
SAN DIEGO,  CA  92121
Correspondent Contact DAN MCKAY
Regulation Number882.1620
Classification Product Code
GWM  
Date Received03/21/1988
Decision Date 05/04/1988
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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