Medical Device Recalls
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1 result found
510(K) Number: K140543 |
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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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PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE Hydrophilic Sheath Introduc... | 2 | 01/05/2017 | Merit Medical Systems, Inc. |
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