FDA 510(k) Applications for Medical Device Product Code: FEG (Tube, Double Lumen For Intestinal Decompression And/Or Intubation)

FDA 510(k) Applications for Medical Device Product Code "FEG"
(Tube, Double Lumen For Intestinal Decompression And/Or Intubation)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K960176	C.R. BARD, INC.	DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER	07/24/1996
K171619	Cook Ireland Ltd	14Fr Colon Decompression Set, Macon Colon Decompression Set	08/01/2017
K053410	KENDALL	GIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTOR	01/06/2006
K040388	KENDALL	NEXT GENERATION SALEM SUMP	05/17/2004
K132314	MEDLINE INDUSTRIES, INC.	MEDLINE ANTI-REFLUX VALVE	09/18/2013
K971354	MICHAEL M. KNOTT, M.D.	KNOTT NG TUBE	11/19/1997