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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 84 Results
510(K) Number: K052115
 
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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
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
1 Step 12 Panel Cup, Item No. NBCA-12M-W 3 12/24/2015 FEI # 3003789989
Ameditech Inc
10-Panel Pipette Drug Screen, Item No. PSP-10M 3 12/24/2015 FEI # 3003789989
Ameditech Inc
11 Panel Dip Card (OPI 300) w/Adult, Item No. 11125AA 3 12/24/2015 FEI # 3003789989
Ameditech Inc
11 Panel Card (OPI 300) w/Adult, Item No. 71125AA 3 12/24/2015 FEI # 3003789989
Ameditech Inc
12-Panel Dip Drug Screen with adulterant, Item No. PSDA-12BUP, PSD-6MTDBO300, PSD-10PPX, PSD-10MOX, ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
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