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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name catheter, intravascular, diagnostic
510(K) Number K913161
Device Name MERIT MANIFOLD
Applicant
MERIT MEDICAL SYSTEMS, INC.
79 west 4500 south
suite 9
salt lake city,  UT  84107
Contact dennis reigle
Regulation Number870.1200
Classification Product Code
DQO  
Date Received07/17/1991
Decision Date 10/21/1991
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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