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U.S. Department of Health and Human Services

Medical Device Recalls
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71 to 80 of 84 Results
510(K) Number: K052115
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ProScreen CLIA Wvd 12 Panel Cup w/Adult., Item No. PSCupA-12M-W ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen Cup CLIA with 6 Panel Drug, Item No. PSCup-6MB-W ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen PSCup-5M Waived, Catalog Number: PSCup-5M Waived Product Usage: The ProScreen Drugs o... 2 11/03/2011 FEI # 3003789989
Ameditech Inc
RealityCHECK Tilt Cup 12 Panel + Adult, Item No. RC12TCA ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU, MTPA-8MBAU These Drugs of Abuse Tests are one-... 2 11/18/2015 FEI # 3003789989
Ameditech Inc
THERMO FISHER 8 DRUG CASSETTE, Item No. MTPA-8MBAU ... 3 12/24/2015 FEI # 3003789989
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 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
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