Medical Device Recalls
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1 result found
510(K) Number: K980135 |
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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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AutoCheck5+, Level 2, specifically designed for Radiometer Americas blood gas analyzers The QUALIC... | 2 | 09/29/2017 | Radiometer America Inc |
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