Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K041874 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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ABL800 Flex Analyzer Model Numbers 393-800 and 393-801 | 2 | 07/01/2022 | Radiometer Medical ApS |
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