Medical Device Recalls
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1 result found
510(K) Number: K082454 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MicroMyst Applicator, Box of 5. Consisting of a multilumen applicator and filtered line for use with... | 1 | 06/20/2025 |
FEI # 3003418325 Integra LifeSciences Corp. (NeuroSciences) |
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