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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 K854157
Device Name PMT ACCUPRESSURE INFUSION SYSTEM 3601
Applicant
Progress Mankind Technology
Box 464
Hopkins,  MN  55343
Applicant Contact ALFRED A IVERSEN
Correspondent
Progress Mankind Technology
Box 464
Hopkins,  MN  55343
Correspondent Contact ALFRED A IVERSEN
Regulation Number880.5725
Classification Product Code
FRN  
Date Received10/11/1985
Decision Date 02/13/1986
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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