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Vygon Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
52
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K151237Nutrisafe 2- ENFit AdaptorFebruary 9, 2016
K141026LEADERFLEXJuly 30, 2014
K121105NUTRISAFE 2 FEEDING TUBEDecember 18, 2012
K100163NUTRISAFE 2 FEEDING TUBES MODEL 362.XXX. 1362.XXXOctober 13, 2011
K073493HEPATOSTAT SETMay 6, 2008
K070705MODIFICATION TO: LATEX-FREE BIONECTOR, MODEL# 896.019, 896.039November 30, 2007
K061796HEPATOSTAT SET, MODEL 760XNovember 2, 2006
K061250MULTICATH EXPERTSeptember 29, 2006
K062425LIFECATH S PICC AND MIDLINE CATHETERSeptember 15, 2006
K060944NUTRISAFE 2September 15, 2006
K052564VYGON LEADER-FLEXApril 5, 2006
K052881VYGON LATEX FREE BIONECTORMarch 2, 2006
K051248VYGON MICRO-ACCESS SAFETY INTRODUCER KITOctober 27, 2005
K051690VYGON NUTRILINE CATHETERSAugust 19, 2005
K041468PREMICATH, 1261.205September 9, 2004
K040657BOUSSIGNAC/VYGON ENDOTRACHEAL TUBE, MODEL 6501.25/30/35 AND 6502.70/75/80June 10, 2004
K013884BOUSSIGNAC C.P.A.P. DEVICEJanuary 21, 2003
K003311NUTRISAFE PUR ENTERAL FEEDING TUBEJanuary 11, 2002
K010913VYGON SPLIT CANNULA INTRODUCERSeptember 28, 2001
K993052VYGON 2 FR EPICUTANEO PUR-CATHETERAugust 3, 2000