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U.S. Department of Health and Human Services

Medical Device Recalls
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81 to 84 of 84 Results
510(K) Number: K052115
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Premier Clia Waived 12 panel Tilt Cup, Item No. C12APC These Drugs of Abuse Tests are one-step im... 2 11/18/2015 FEI # 3003789989
Ameditech Inc
ProScreen 10 Drug Panel Cassette Test, Item No. CPSP-10PPX; ProScreen 10 Panel Cup, Item No. PSCup-... 2 11/18/2015 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
ProScreen PSCup-5M Waived, Catalog Number: PSCup-5M Waived Product Usage: The ProScreen Drugs o... 2 11/03/2011 FEI # 3003789989
Ameditech Inc
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