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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 K922637
Device Name HORIZON PUMP Y-TYPE BLOOD SET
Applicant
MCGAW, INC.
2525 MCGAW AVE.
P.O. BOX 19791
IRVINE,  CA  92713 -9791
Applicant Contact DIANE GERST
Correspondent
MCGAW, INC.
2525 MCGAW AVE.
P.O. BOX 19791
IRVINE,  CA  92713 -9791
Correspondent Contact DIANE GERST
Regulation Number880.5440
Classification Product Code
FPA  
Date Received06/04/1992
Decision Date 06/04/1993
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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