Medical Device Recalls
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1 result found
510(K) Number: K934697 |
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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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| MaxForce TTS High Performance Esophageal Balloon Dilatation Catheter 8mm/24 Fr | 2 | 05/15/2003 | Boston Scientific Corporation |
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