Medical Device Recalls
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1 result found
510(K) Number: K040713 |
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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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Transseptal Sheath Introducer Kits (under trade names: HeartSpan, Channel FX, Torflex, Braided Guidi... | 1 | 03/04/2010 | Thomas Medical Products Inc |
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