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FEG — Tube, Double Lumen For Intestinal Decompression And/Or Intubation Class II

FDA Device Classification

Classification Details

Product Code
FEG
Device Class
Class II
Regulation Number
876.5980
Submission Type
Review Panel
GU
Medical Specialty
Gastroenterology, Urology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K171619cook ireland14Fr Colon Decompression Set, Macon Colon Decompression SetAugust 1, 2017
K132314medline industriesMEDLINE ANTI-REFLUX VALVESeptember 18, 2013
K053410kendallGIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTORJanuary 6, 2006
K040388kendallNEXT GENERATION SALEM SUMPMay 17, 2004
K971354michael m. knott, m.dKNOTT NG TUBENovember 19, 1997
K960176c.r. bardDAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTERJuly 24, 1996
K926073surgimarkULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBEMay 15, 1995
K935781sherwood medicalARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAYJanuary 27, 1995
K921104icu medicalLOPEZ VALVE WITH NG SUMP TUBEOctober 26, 1992
K900035wilson-cook medicalWILSON-COOK COLON DECOMPRESSION SETMarch 7, 1990
K880850kmb medical productsKEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVEMay 26, 1988
K772282mallinckrodt critical careHODGE TUBEMarch 9, 1978
K771048axiom medicalCATHETERS, DRAINAGEJuly 19, 1977