Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K193248 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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SIEMENS Biograph Vision: a) 450, b) 600, c) 600 Edge | 2 | 02/13/2023 | Siemens Medical Solutions USA, Inc. |
SIEMENS Biograph mCT: a) Flow 64-4R Seismic, b) S(40)-3R Seismic, c) S(64)-3R Seismic, d) S(40)-4R ... | 2 | 02/13/2023 | Siemens Medical Solutions USA, Inc. |
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