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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Container, I.V.
510(k) Number K932649
Device Name PHARMAFEED
Applicant
Plasco, Inc.
3849 Swanson St.
Gurnee,  IL  60031
Applicant Contact GARY S BOTSFORD
Correspondent
Plasco, Inc.
3849 Swanson St.
Gurnee,  IL  60031
Correspondent Contact GARY S BOTSFORD
Regulation Number880.5025
Classification Product Code
KPE  
Date Received06/02/1993
Decision Date 11/16/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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