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U.S. Department of Health and Human Services

Medical Device Recalls
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51 to 60 of 84 Results
510(K) Number: K052115
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Product Description
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ProScreen 6 Panel Dip Drug Screen, Item No. PSD-6BUPO3 ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen 7 Panel Dip Card, Item No. PSD-7MPB, PSD-7MO, PSD-7M ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen 8 Panel Dip Card, Item No. PSD-8P ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen 8 Panel Dip Card w/Adult, Item No. PSDA-8P, PSDA-8MBO300 ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen 9 Panel Cup w/Adulterants, Item No. PSCUPA-9BO300 ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen CLIA Waived Cup 6 Drugs w/Adul, Item No. PSCupA-6MB-W ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen CLIA Waived Cup with 6 Drugs, Item No. PSCup-6BO-W ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen CLIA Waived Cup with 8 Drug, Item No. PSCup-8P-W ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
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
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