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U.S. Department of Health and Human Services

Medical Device Recalls
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51 to 60 of 79 Results
510(K) Number: K113501
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ProScreen 9 Panel Cup w/Adulterants, Item No. PSCUPA-9BO300 ... 3 12/24/2015 Ameditech Inc
ProScreen CLIA Waived Cup 6 Drugs w/Adul, Item No. PSCupA-6MB-W ... 3 12/24/2015 Ameditech Inc
ProScreen CLIA Waived Cup with 6 Drugs, Item No. PSCup-6BO-W ... 3 12/24/2015 Ameditech Inc
ProScreen CLIA Waived Cup with 8 Drug, Item No. PSCup-8P-W ... 3 12/24/2015 Ameditech Inc
ProScreen CLIA Wvd 12 Panel Cup w/Adult., Item No. PSCupA-12M-W ... 3 12/24/2015 Ameditech Inc
ProScreen Cup CLIA with 6 Panel Drug, Item No. PSCup-6MB-W ... 3 12/24/2015 Ameditech Inc
RealityCHECK Tilt Cup 12 Panel + Adult, Item No. RC12TCA ... 3 12/24/2015 Ameditech Inc
THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU ... 3 12/24/2015 Ameditech Inc
THERMO FISHER 8 DRUG CASSETTE, Item No. MTPA-8MBAU ... 3 12/24/2015 Ameditech Inc
1 Step 12 Panel Cup, Item No. NBCA-12M-W These Drugs of Abuse Tests are one-step immunoassays for t... 2 11/18/2015 Ameditech Inc
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