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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Computer, Blood-Pressure
510(k) Number K912833
Device Name CAMINO MODEL M420: MONIT INTER W/MEAN PRES DISPLAY
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 Number870.1110
Classification Product Code
DSK  
Date Received06/26/1991
Decision Date 09/23/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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