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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name introducer, catheter
510(k) Number K840455
Device Name EMERGENCY INFUSION DEVICE
Original Applicant
ARROW INTL., INC.
Regulation Number870.1340
Classification Product Code
DYB  
Date Received02/02/1984
Decision Date 05/23/1984
Decision substantially equivalent (SE)
Classification Advisory Committee Cardiovascular
Review Advisory Committee Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
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