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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stopcock, I.V. Set
510(k) Number K850280
Device Name VIGGO CONNECTA 3-WAY INFUSION STOPCOCK
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
FMG  
Date Received01/23/1985
Decision Date 04/11/1985
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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