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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 84 Results
510(K) Number: K113046
 
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iCup Drug Screen Cup, Item No. I-DXA-187-016, I-DXA-167-013; iCup DX 10 Panel w/Adulterant, Item No... 2 11/18/2015 Ameditech Inc
iCup DX 8 Panel w/Adulterant, Item No. I-DXA-187-016 3 12/24/2015 Ameditech Inc
iCup DX 6 Panel w/Adulterant, Item No. I-DXA-167-013 3 12/24/2015 Ameditech Inc
iCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023 3 12/24/2015 Ameditech Inc
iCup DX 11 Panel w/ Adulterant, Item No. I-DXA-1117-131 3 12/24/2015 Ameditech Inc
iCup DX 10 Panel w/Adulterant, Item No. I-DXA-1107-142 3 12/24/2015 Ameditech Inc
The Drug Detection Agency 6 Panel Cup Body and Lid w/Adult (AU), Item No. TDDA-6MBAU-CUP These ... 2 11/18/2015 Ameditech Inc
THERMO FISHER 8 DRUG CASSETTE, Item No. MTPA-8MBAU ... 3 12/24/2015 Ameditech Inc
THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU, MTPA-8MBAU These Drugs of Abuse Tests are one-... 2 11/18/2015 Ameditech Inc
THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU ... 3 12/24/2015 Ameditech Inc
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