Medical Device Recalls
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1 result found
510(K) Number: K161128 |
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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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| Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Endure Negative Pressure W... | 2 | 07/23/2018 |
FEI # 1419937 Medela Inc |
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