Medical Device Recalls
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1 result found
510(K) Number: K071145 |
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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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Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for bloo... | 2 | 10/23/2015 | Nipro Medical Corporation |
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