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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 K943770
Device Name LOW VOLUME MULTIPORT
Applicant
B. BRAUN OF AMERICA, INC.
824 TWELFTH AVE.
PO BOX 4027
BETHLEHEM,  PA  18018 -0027
Applicant Contact MARK S ALSBERGE
Correspondent
B. BRAUN OF AMERICA, INC.
824 TWELFTH AVE.
PO BOX 4027
BETHLEHEM,  PA  18018 -0027
Correspondent Contact MARK S ALSBERGE
Regulation Number880.5440
Classification Product Code
FPA  
Date Received08/02/1994
Decision Date 04/10/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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