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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 K930222
Device Name CAMINO VENTRICULAR ACCESS DEVICE
Applicant
CAMINO LABORATORIES, INC.
5955 PACIFIC CENTER BLVD.
SAN DIEGO,  CA  92121
Applicant Contact HAZEL M AKER
Correspondent
CAMINO LABORATORIES, INC.
5955 PACIFIC CENTER BLVD.
SAN DIEGO,  CA  92121
Correspondent Contact HAZEL M AKER
Regulation Number882.5550
Classification Product Code
JXG  
Date Received01/15/1993
Decision Date 04/15/1993
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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