FDA 510(k) Application Details - K841788

Device Classification Name Transducer, Blood-Pressure, Extravascular

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510(K) Number K841788
Device Name Transducer, Blood-Pressure, Extravascular
Applicant UTAH MEDICAL PRODUCTS, INC.
1212 EAST 60 SOUTH
LEHI, UT US
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Contact EDWIN O GOODMAN
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Regulation Number 870.2850

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Classification Product Code DRS
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Date Received 04/30/1984
Decision Date 03/25/1985
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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