FDA 510(k) Application Details - K893232

Device Classification Name Computer, Blood-Pressure

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510(K) Number K893232
Device Name Computer, Blood-Pressure
Applicant CAMINO LABORATORIES, INC.
5955 PACIFIC CENTER BLVD.
SAN DIEGO, CA US
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Contact HAZEL SHUMWAY
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Regulation Number 870.1110

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Classification Product Code DSK
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Date Received 04/28/1989
Decision Date 07/14/1989
Decision SE - Substantially Equivalent
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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