Medical Device Recalls
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1 result found
510(K) Number: K041297 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Test Strips packaged in the OC-Light Manual iFOBT Kit, Catalog No. FOB50. For the rapid, qualitat... | 2 | 04/04/2013 | Polymedco, Inc |
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