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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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Immutest 11 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-11OP ... 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 5 Pnl Drug Cup w/ Adult -waived, Item No. IMCA-5AB-W ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
Immutest Cup CLIA Waived w/Adulteration, Item No. IMCA-7MT-W ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
Micro Screen 6 Panel Cup with Adult (AU), Item No. MSCA-6MBAU ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
Micro Screen 6 Panel Cup with Adult (AU), Item No. MSCA-6MBAU These Drugs of Abuse Tests are one-... 2 11/18/2015 FEI # 3003789989
Ameditech Inc
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
ProScProScreen 10 Panel Cup with Adulterants, Item No. PSCupA-10AM ... 3 12/24/2015 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
ProScreen 10 Drug Panel Cassette Test, Item No. PSP-10PPX ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
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