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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name set, administration, intravascular
510(K) Number K031923
Device Name ULTRASITE VALVE
Applicant
B. BRAUN MEDICAL, INC.
901 marcon blvd.
allentown,  PA  18109
Contact sheri l musgnung
Regulation Number880.5440
Classification Product Code
FPA  
Date Received06/23/2003
Decision Date 08/11/2003
Decision substantially equivalent (SE)
Classification Advisory Committee General Hospital
Review Advisory Committee General Hospital
summary summary
Type Traditional
Reviewed by Third Party No
Expedited Review No
Combination Product No
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