Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K001009 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| POLYMEDCO ULTRA-CRP LATEX ENHANCED ASSAY, Catalog No. CPU400. Contents: 1 x 50 ML R1, 2 x 6 ML R2. ... | 3 | 01/06/2004 |
FEI # 1000119795 Polymedco, Inc |
| POLYMEDCO ULTRA-CRP High Sensitive Assay For the DIMENSION(R) systems, Catalog No. USC300. Contents:... | 3 | 01/06/2004 |
FEI # 1000119795 Polymedco, Inc |
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