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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Cannula, Ventricular
510(k) Number K920088
Device Name CAMINO VENTRICULAR NEEDLE
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 Number882.4060
Classification Product Code
HCD  
Date Received01/08/1992
Decision Date 05/01/1992
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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