Medical Device Recalls
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1 result found
510(K) Number: K013919 |
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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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Torflex Transseptal Guiding Sheath, Baylis Medical Company Inc., 5959 Trans-Canada Highway, Montreal... | 1 | 03/10/2010 | Baylis Medical Corp * |
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