Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K812574 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Liquid HDL (PEG) Cholesterol Reagent, Pointe Scientific, Inc, Canton, MI; Catalog # 7-H7511-30, 8-H7... | 2 | 02/25/2010 |
FEI # 1827821 Pointe Scientific, Inc. |
| Liquid HDL (PEG) Cholesterol Reagent Set. Pointe Scientific HDL Cholesterol Reagent Set, Pointe Sci... | 2 | 02/25/2010 |
FEI # 1827821 Pointe Scientific, Inc. |
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