FDA 510(k) Application Details - K760738

Device Classification Name System, Measurement, Blood-Pressure, Non-Invasive

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510(K) Number K760738
Device Name System, Measurement, Blood-Pressure, Non-Invasive
Applicant MEDICAL MONITORS, INC.

, US
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Regulation Number 870.1130

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Classification Product Code DXN
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Date Received 09/28/1976
Decision Date 01/21/1977
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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