Medical Device Recalls
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1 result found
510(K) Number: K091591 |
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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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| ProVu Single Use Video Stylet with ET Tube, Part/Size: 038-990-080U/ 8.0, 038-990-075U/ 7.5, 038-990... | 1 | 11/26/2020 |
FEI # 3006363476 Flexicare Medical Ltd. |
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