Medical Device Recalls
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1 result found
510(K) Number: K071227 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Turbo Elite 0.9mm Turbo Elite (TE) RX, Model #410-154, tip diameter 0.9mm/.038 in, 4 Fr, sterile EO.... | 3 | 02/11/2009 | Spectranetics Corporation |
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