Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K032306 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| VersaTREK Windows Software, Version 5.4.3 is a component of the VersaTrek System. The Software CD wi... | 3 | 09/06/2012 |
FEI # 1000515493 Trek Diagnostic Systems |
| Thermo Scientific VersaTREK REDOX 1, Ref 7102-44, 80ml with Stir Bar (O2 aerobic), 50 bottles/box, I... | 2 | 07/15/2014 |
FEI # 1924669 Remel Inc |
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