Medical Device Recalls
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1 result found
510(K) Number: K213829 |
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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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SCENARIA View: Software Version V1.08, V1.09B, V1.09C, V1.09D, V1.0B, V1.0C | 2 | 09/16/2022 | FUJIFILM Healthcare Americas Corporation |
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