FDA 510(k) Application Details - K870301

Device Classification Name Transducer, Blood-Pressure, Extravascular

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510(K) Number K870301
Device Name Transducer, Blood-Pressure, Extravascular
Applicant MEDEX, INC.
3637 LACON RD.
HILLARD, OH US
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Contact MARK T SONDRINI
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Regulation Number 870.2850

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Classification Product Code DRS
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Date Received 01/28/1987
Decision Date 05/06/1987
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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