Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K024050 |
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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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Ascend® AQ® Ureteral Dilation Balloon Catheter Set The Ascend® AQ® Ureteral Dilation Balloon Cathet... | 2 | 03/24/2016 | Cook Inc. |
UltraxxTM Nephrostomy Balloon Set The Ultraxx" Nephrostomy Balloon Set consists of a radiopaque bal... | 2 | 03/24/2016 | Cook Inc. |
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