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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Transducer, Blood-Pressure, Extravascular
510(k) Number K841788
Device Name UTAH DISPOSABLE PRESSURE TRANSDUCER
Applicant
UTAH MEDICAL PRODUCTS, INC.
1212 EAST 60 SOUTH
LEHI,  UT  84043 -
Applicant Contact EDWIN O GOODMAN
Correspondent
UTAH MEDICAL PRODUCTS, INC.
1212 EAST 60 SOUTH
LEHI,  UT  84043 -
Correspondent Contact EDWIN O GOODMAN
Regulation Number870.2850
Classification Product Code
DRS  
Date Received04/30/1984
Decision Date 03/25/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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