Medical Device Recalls
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1 result found
510(K) Number: K990222 |
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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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| IMMULITE 2000 Systems HCG [200 Tests, material number 10381206, catalog number L2KCG] and [600 Tests... | 2 | 04/28/2022 |
FEI # 2432235 Siemens Healthcare Diagnostics, Inc. |
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