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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Pump, Infusion
510(k) Number K872514
Device Name INFUSION PUMP MODEL 270
Applicant
Avi, Inc.
1120 Red Fox Rd.
St. Paul,  MN  55112
Applicant Contact J SUEDKAMP
Correspondent
Avi, Inc.
1120 Red Fox Rd.
St. Paul,  MN  55112
Correspondent Contact J SUEDKAMP
Regulation Number880.5725
Classification Product Code
FRN  
Date Received06/24/1987
Decision Date 12/16/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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