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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 84 Results
510(K) Number: K052115
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6 Panel Cup Body and Lid w/Adult (AU), Item No. TDDA-6MBAU-CUP 3 12/24/2015 FEI # 3003789989
Ameditech Inc
BZO Strip Dip Card (300ng/ml)*, Item No. 100170 3 12/24/2015 FEI # 3003789989
Ameditech Inc
CLIA RDTC 12-Panel Cup (w/Adulteration), Item No. CLIA-RDTC-12, DCC-81205-5 3 12/24/2015 FEI # 3003789989
Ameditech Inc
DrugCheck Waived 12 Panel Cup w/Adult, Item No. DCC-81205-5 3 12/24/2015 FEI # 3003789989
Ameditech Inc
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
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