Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K031873 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Cardiac Marker Control Level 1, List Number 136601-06F12-02; Cardiac Marker Control Level 2, List nu... | 2 | 04/01/2011 | Abbott Point Of Care Inc. |
| Cardiac Marker Control Calibration Verification Set, List number 136604/06F15-02. Used to verify ... | 2 | 04/01/2011 | Abbott Point Of Care Inc. |
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