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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 84 Results
510(K) Number: K052115
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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
iCup DX 11 Panel w/ Adulterant, Item No. I-DXA-1117-131 3 12/24/2015 FEI # 3003789989
Ameditech Inc
iCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023 3 12/24/2015 FEI # 3003789989
Ameditech Inc
iCup DX 6 Panel w/Adulterant, Item No. I-DXA-167-013 3 12/24/2015 FEI # 3003789989
Ameditech Inc
iCup DX 8 Panel w/Adulterant, Item No. I-DXA-187-016 3 12/24/2015 FEI # 3003789989
Ameditech Inc
Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5 ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
Immutest 11 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-11OP ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
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