Medical Device Recalls
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1 result found
510(K) Number: K123640 |
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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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| TX1 Tissue Removal System. TX1 Procedure Pack P/N 554-1003-001 (outer box), TX1 MicroTip P/N 554-10... | 2 | 05/06/2014 |
FEI # 1000135560 Tenex Health Inc |
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