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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name catheter, intravascular, therapeutic, short-term less than 30 days
510(k) Number K850276
Device Name VIGGO NEOFLON INFUSION CANNULA
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 Number880.5200
Classification Product Code
FOZ  
Date Received01/23/1985
Decision Date 04/12/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
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