Tube, Double Lumen For Intestinal Decompression And/Or Intubation
FDA product code FEG · 13 cleared devices
Class 2
Gastroenterology, Urology
- Regulation
- 21 CFR 876.5980
- Review panel
- GU
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1977-07-19 – 2017-08-01
FEG
2017-08-01
FEG
2013-09-18
MEDLINE ANTI-REFLUX VALVE
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FEG
2006-01-06
GIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTOR
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FEG
2004-05-17
NEXT GENERATION SALEM SUMP
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FEG
1997-11-19
KNOTT NG TUBE
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FEG
1996-07-24
DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER
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FEG
1995-05-15
ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBE
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FEG
1995-01-27
ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY
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FEG
1992-10-26
LOPEZ VALVE WITH NG SUMP TUBE
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FEG
1990-03-07
WILSON-COOK COLON DECOMPRESSION SET
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FEG
1988-05-26
KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE
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FEG
1978-03-09
HODGE TUBE
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FEG
1977-07-19
CATHETERS, DRAINAGE
View details →No matching devices.
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