Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K041874 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ABL800 FLEX model number 393-800 and 393-801, UDI:(01)05700693938004 | 2 | 05/01/2020 | Radiometer Medical ApS |
ABL800 FLEX, model number/UDI 393-800/0570 In Vitro testing of samples of whole blood for the param... | 2 | 04/08/2020 | Radiometer Medical ApS |
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