Medical Device Recalls
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1 result found
510(K) Number: K210066 |
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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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ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing and presentation of medi... | 2 | 01/14/2022 | Konica Minolta Healthcare Americas, Inc. |
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