FEG · Class II · 21 CFR 876.5980

FDA Product Code FEG: Tube, Double Lumen For Intestinal Decompression And/or Intubation

Leading manufacturers include Medline Industries, Inc., Mallinckrodt Critical Care and Wilson-Cook Medical, Inc..

13
Total
13
Cleared
190d
Avg days
1977
Since

FDA 510(k) Cleared Tube, Double Lumen For Intestinal Decompression And/or Intubation Devices (Product Code FEG)

13 devices
1–13 of 13
Cleared Sep 18, 2013
MEDLINE ANTI-REFLUX VALVE
K132314
Medline Industries, Inc.
Gastroenterology & Urology · 55d
Cleared Jul 24, 1996
DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER
K960176
C.R. Bard, Inc.
Gastroenterology & Urology · 190d
Cleared Jan 27, 1995
ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY
K935781
Sherwood Medical Co.
Gastroenterology & Urology · 417d
Cleared Oct 26, 1992
LOPEZ VALVE WITH NG SUMP TUBE
K921104
Icu Medical, Inc.
Gastroenterology & Urology · 231d
Cleared Mar 07, 1990
WILSON-COOK COLON DECOMPRESSION SET
K900035
Wilson-Cook Medical, Inc.
Gastroenterology & Urology · 64d
Cleared Mar 09, 1978
HODGE TUBE
K772282
Mallinckrodt Critical Care
Gastroenterology & Urology · 87d

About Product Code FEG - Regulatory Context