Medical Device Recalls
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1 result found
510(K) Number: K131300 |
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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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POWERWAND Safety Introducer with Extended Dwell Catheter; Catalog no. 92006. Used to gain access... | 2 | 09/18/2013 | Access Scientific Inc |
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