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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 K850769
Device Name VIGGO ACCESSORIES FOR I.V. THERAPY
Applicant
Viggo Products
Ohmeda
P.O. Box 7550
Madison,  WI  53707
Applicant Contact RAYMOND T RIDDLE
Correspondent
Viggo Products
Ohmeda
P.O. Box 7550
Madison,  WI  53707
Correspondent Contact RAYMOND T RIDDLE
Regulation Number880.5440
Classification Product Code
FPA  
Date Received02/25/1985
Decision Date 05/29/1985
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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