Medical Device Recalls
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1 result found
510(K) Number: K070669 |
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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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| Product Name: nanoPOINT Injector System, item number 37-0000-08. Intended to fold and insert a ST... | 2 | 08/20/2013 |
FEI # 3006151006 Medicel Ag |
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