Medical Device Recalls
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1 result found
510(K) Number: K991431 |
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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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Two Lumen 14F Hemodialysis Catheter Kits/Sets with Blue FlexTip Arrowg+ard Blue Curved Catheter for ... | 2 | 07/20/2004 | Arrow International Inc |
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