Medical Device Recalls
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21 to 21 of 21 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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pCO2 D788 Membranes. Distributed by Radiometer America, Inc., Westlake, OH. An automatic or semi-... | 2 | 02/24/2014 | Radiometer America Inc |
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