Medical Device Recalls
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1 result found
510(K) Number: K202335 |
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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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Ambra PACS, Ambra ProViewer. Software for use as a primary diagnostic and analysis tool for diagnos... | 2 | 09/27/2022 | DICOM Grid, Inc. d/b/a Ambra Health |
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