Medical Device Recalls
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1 result found
510(K) Number: K970159 |
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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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Flex-Neck Classic Peritoneal Dialysis Catheter (Pediatric) Product Usage: If the patient is a su... | 2 | 08/15/2018 | Merit Medical Systems, Inc. |
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