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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 40 of 84 Results
510(K) Number: K052115
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EDI BZO Uncut Sheet - Cup*, Item No. 160170 3 12/24/2015 FEI # 3003789989
Ameditech Inc
First Check 1 Panel Drug Cup: (THC); AMT Item Number 990400B 2 09/30/2020 FEI # 3003789989
Ameditech Inc
First Check 2 Panel Drug Cup: (THC/COC); AMT Item Number 990600B 2 09/30/2020 FEI # 3003789989
Ameditech Inc
First Check 4 Panel Drug Cup: COC/MET1000/OPI2000/THC): (THC/COC); AMT Item Number 990100B 2 09/30/2020 FEI # 3003789989
Ameditech Inc
First Check 7 Panel Drug Cup: (AMP/COC/MDMA/MET/OPI/PCP/THC); AMT Item Number 990100B 2 09/30/2020 FEI # 3003789989
Ameditech Inc
ImmuTest 12 Panel Dip Card, Item No. IMD-12MO3 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ImmuTest Cup 7-panel w/ Adulteration, Item No. IMCA-7P ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ImmuTest Drugs of Abuse Cup (AMT Item Number/ AMT Description): IMCA-5AB-W / "ImmuTest Drugs of A... 2 09/30/2020 FEI # 3003789989
Ameditech Inc
Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5 ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5; Immutest 11 Pnl Drug Screen Cup w/ Ad... 2 11/18/2015 FEI # 3003789989
Ameditech Inc
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