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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 50 of 84 Results
510(K) Number: K052115
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Product Description
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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
Immutest 5 Pnl Drug Cup w/ Adult -waived, Item No. IMCA-5AB-W ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
Immutest 12 Panel Cup w/Adulteration, Item No. IMCA-11OP ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ImmuTest 12 Panel Dip Card, Item No. IMD-12MO3 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ImmuTest Cup 7-panel w/ Adulteration, Item No. IMCA-7P ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
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