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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Arterial Blood Sampling Kit
510(k) Number K955663
Device Name ABC IN-LINE BLOOD SAMPLING KIT
Applicant
UTAH MEDICAL PRODUCTS, INC.
7043 SOUTH 300 WEST
MIDVALE,  UT  84047 -1048
Applicant Contact JOHN W SMITH
Correspondent
UTAH MEDICAL PRODUCTS, INC.
7043 SOUTH 300 WEST
MIDVALE,  UT  84047 -1048
Correspondent Contact JOHN W SMITH
Regulation Number868.1100
Classification Product Code
CBT  
Date Received12/13/1995
Decision Date 03/17/1997
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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