Medical Device Recalls
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1 result found
510(K) Number: K113680 |
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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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AxoTrack I Sterile Procedure Kit 18G, K1001-18XTW, (24/case labeled for US, 5/case labeled for US, 2... | 2 | 12/16/2014 | Soma Access Systems LLC |
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