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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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First Check 1 Panel Drug Cup: (THC); AMT Item Number 990400B 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
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 2 Panel Drug Cup: (THC/COC); AMT Item Number 990600B 2 09/30/2020 FEI # 3003789989
Ameditech Inc
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