Medical Device Recalls
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1 result found
510(K) Number: K021723 |
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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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Sheath Adapter with Cath-Gard® Catheter Contamination Shield for use with 4 - 7 Fr. Catheters; Produ... | 2 | 05/30/2018 | Arrow International Inc |
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