FCDClass I
Barium Enema Kit
Gastroenterology, Urology · 21 CFR 876.5210
This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
MDR events16All time
Recalls0All time
Registered firms2Currently listed
510(k) clearances2All time
Recent MDR events
16 adverse event reports on file
- AIR TIPMay 16, 2008Malfunction1827430-2008-00001
- EZEMMay 21, 2007MalfunctionE-z-em Inc.MW5001941
- E-Z BARIUM ENEMA TIPSep 19, 2000MalfunctionE-z-em, Inc.2432460-2000-00029
- E-Z BARIUM ENEMA TIPSep 19, 2000E-z-em, Inc.2432460-2000-00031
- E-Z BARIUM ENEMA TIPSep 19, 2000MalfunctionE-z-em, Inc.2432460-2000-00030
- EZEM SUPER XL ENEMA BAG SYSTEMAug 15, 2000InjuryEzemMW1019656
- SUPER XL DELIVERY SYSTEMSep 27, 1999InjuryE-z-em, Inc.2647856-1999-00040
- E-Z-EM BARIUM SOLUTION PREFILLED ENEMA BAGAug 5, 1999InjuryE-z-em, Inc.MW1016891
- EZ-EMSep 5, 1997DeathEz-em, Inc.MW1012034
- SUPER XL DELIVERY SYSTEM FOR AIR CONTRAST STUDIESAug 25, 1997InjuryE-z-em, Caribe2411512-1997-00004
Event type breakdown
Malfunction7
Injury6
Unspecified2
Death1
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
2 firms currently registered for this product code
510(k) clearances
2 clearances for this product code