Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K181185 |
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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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Change Healthcare Enterprise Viewer - Product Usage: intended to be used with off-the-shelf hardware... | 2 | 06/02/2021 | CHANGE HEALTHCARE CANADA COMPANY |
Change Healthcare Enterprise Viewer | 2 | 04/28/2021 | CHANGE HEALTHCARE CANADA COMPANY |
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