Medical Device Recalls
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1 result found
510(K) Number: K203572 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| KARL STORZ Radel Sterilization Trays, Models: 27717A, 27717B, 39301A, 39301C, 39231XA, 39301C1, 3931... | 2 | 06/21/2023 |
FEI # 3007475226 Karl Storz Endoscopy |
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