Medical Device Recalls
-
71 to 79 of 79 Results
510(K) Number: K113501 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU, MTPA-8MBAU These Drugs of Abuse Tests are one-... | 2 | 11/18/2015 | Ameditech Inc |
THERMO FISHER 8 DRUG CASSETTE, Item No. MTPA-8MBAU ... | 3 | 12/24/2015 | Ameditech Inc |
The Drug Detection Agency 6 Panel Cup Body and Lid w/Adult (AU), Item No. TDDA-6MBAU-CUP These ... | 2 | 11/18/2015 | Ameditech Inc |
iCup DX 10 Panel w/Adulterant, Item No. I-DXA-1107-142 | 3 | 12/24/2015 | Ameditech Inc |
iCup DX 11 Panel w/ Adulterant, Item No. I-DXA-1117-131 | 3 | 12/24/2015 | Ameditech Inc |
iCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023 | 3 | 12/24/2015 | Ameditech Inc |
iCup DX 6 Panel w/Adulterant, Item No. I-DXA-167-013 | 3 | 12/24/2015 | Ameditech Inc |
iCup DX 8 Panel w/Adulterant, Item No. I-DXA-187-016 | 3 | 12/24/2015 | Ameditech Inc |
iCup Drug Screen Cup, Item No. I-DXA-187-016, I-DXA-167-013; iCup DX 10 Panel w/Adulterant, Item No... | 2 | 11/18/2015 | Ameditech Inc |
-