FDA 510(k) Application Details - K812639

Device Classification Name Transducer, Vessel Occlusion

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510(K) Number K812639
Device Name Transducer, Vessel Occlusion
Applicant FRONTIER PRODUCTS

, US
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Regulation Number 870.2890

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Classification Product Code DXP
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Date Received 09/16/1981
Decision Date 10/02/1981
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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