FDA 510(k) Application Details - K791838

Device Classification Name Computer, Blood-Pressure

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510(K) Number K791838
Device Name Computer, Blood-Pressure
Applicant MEDTEL PTY. LTD.

, US
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Regulation Number 870.1110

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Classification Product Code DSK
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Date Received 09/14/1979
Decision Date 10/01/1979
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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