Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K041635 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| in2it (I) and (II) System A1c Test cartridges and in2it Self Test System A1c Test Cartridges, for us... | 2 | 10/22/2010 | Bio-Rad Laboratories Inc |
| in2it (I) A1c Test Cartridges (Catalog 281-0001EX) and in2it (II) A1c Test Cartridges (Catalog 281-0... | 2 | 10/21/2010 | Bio-Rad Laboratories Inc |
| Cholestech GDX A1C Test Cartridge. The Cholestech GDX A1C Test is an in-vitro diagnostic test that ... | 2 | 09/23/2008 | Cholestech Corp |
| Product is in2it A1C In-Office Analyzer Test Cartridge. Catalogue number is 902074P (Test Cartridge... | 2 | 11/18/2005 | Provalis Diagnostics |
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