Medical Device Recalls
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1 result found
510(K) Number: K050232 |
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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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RigiflexTM 11 Single-Use Achalasia Balloon Dilator, Material Number (UPN) M00554510 Product Usage... | 3 | 07/10/2013 | Boston Scientific Corporation |
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