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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 K885030
Device Name STANDARD ADMINISTRATION SETS
Applicant
3M COMPANY
1120 RED FOX RD.
ST. PAUL,  MN  55112
Applicant Contact J SUEDKAMP
Correspondent
3M COMPANY
1120 RED FOX RD.
ST. PAUL,  MN  55112
Correspondent Contact J SUEDKAMP
Regulation Number880.5440
Classification Product Code
FPA  
Date Received12/05/1988
Decision Date 01/24/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
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