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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name shunt, central nervous system and components
510(k) Number K932769
Device Name CAMINO VENTRICULAR DRAINAGE SYSTEM
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 Number882.5550
Classification Product Code
JXG  
Date Received06/08/1993
Decision Date 03/30/1995
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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