Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K011968 |
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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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Boston Scientific, Fort®® Guide Wire, Floppy, 300cm x 2 cm REF 34949-04, for use in intravascular i... | 2 | 06/24/2009 | Boston Scientific Corporation |
Boston Scientific Fort®® Guide Wire, Floppy Marker Wire, 300cm x 2 cm, REF 34949-02, for use in intr... | 2 | 06/24/2009 | Boston Scientific Corporation |
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