Medical Device Recalls
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1 result found
510(K) Number: K040228 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonogr... | 2 | 02/26/2018 |
FEI # 3010790133 Medistim Asa |
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