Medical Device Recalls
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1 result found
510(K) Number: K083386 |
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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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| Atellica CH Calcium_2 (CA_2), Siemens Material Number 11097644 | 2 | 04/14/2022 |
FEI # 2432235 Siemens Healthcare Diagnostics, Inc. |
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