Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Medical Device Recalls
  • Print
  • Share
  • E-mail
-
31 to 40 of 84 Results
510(K) Number: K052115
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 > 
Results per Page
New Searchexport reports to excelExport to Excel | HelpHelp
Product Description
Sort by Product Name [A-Z]
Sort by Product Name [Z-A]
Recall
Class
Sort by Recall Class [0-9]
Sort by Recall Class [9-0]
FDA Recall
Posting Date
Sort by Date Classified [0-9]
Sort by Date Classified [9-0]
Recalling Firm
Sort by Recalling Firm [A-Z]
Sort by Recalling Firm [Z-A]
DrugSmart 10 Test Cup (PCP & OXY), Item No. 61020D 3 12/24/2015 FEI # 3003789989
Ameditech Inc
DrugSmart 11 Test Cup, Item No. 61127D 3 12/24/2015 FEI # 3003789989
Ameditech Inc
DrugSmart 12 Test Cup (Multi & BUP), Item No. 61210D DrugSmart 12 Test Cup (Multi/Single/BUP), Item... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
DrugSmart 9 Test Cup (BUP), Item No. 60960D 3 12/24/2015 FEI # 3003789989
Ameditech Inc
DrugSmart Cup 10, Item No. 61093D-3C, 61085D, 61015D 3 12/24/2015 FEI # 3003789989
Ameditech Inc
DrugSmart Cup THC/COC/AMP//MET/OPI2/BZO, Item No. 60600D 3 12/24/2015 FEI # 3003789989
Ameditech Inc
DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC, Item No. 30600D 3 12/24/2015 FEI # 3003789989
Ameditech Inc
DrugSmart Dip AMP/OPI2/COC/THC/BZO Test, Item No. 30520D 3 12/24/2015 FEI # 3003789989
Ameditech Inc
EDI BZO Uncut Sheet - Cup*, Item No. 160170 3 12/24/2015 FEI # 3003789989
Ameditech Inc
iCup DX 10 Panel w/Adulterant, Item No. I-DXA-1107-142 3 12/24/2015 FEI # 3003789989
Ameditech Inc
-
-