Medical Device Recalls
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1 result found
510(K) Number: K963257 |
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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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Peripherally Inserted Midline Catheter Kit with Placement Wire, REF MK-02031-TW Product Usage: T... | 2 | 07/08/2018 | Arrow International Inc |
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