Medical Device Recalls
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1 result found
510(K) Number: K201373 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For use in obtaining diagno... | 2 | 03/02/2023 | Carestream Health, Inc. |
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