FDA 510(k) Application Details - K896535

Device Classification Name Computer, Blood-Pressure

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510(K) Number K896535
Device Name Computer, Blood-Pressure
Applicant OXFORD MEDILOG, INC.
11526 53RD. ST. N.
CLEARWATER, FL US
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Contact MICHAEL J SMITH
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Regulation Number 870.1110

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Classification Product Code DSK
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Date Received 11/14/1989
Decision Date 01/18/1990
Decision SE - Substantially Equivalent
Classification Advisory Committee AN - Anesthesiology
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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