Medical Device Recalls
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1 result found
510(K) Number: K030613 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US, CAT 8100E1-US, CAT 8100EP1, C... | 2 | 09/22/2026 |
FEI # 3012238587 Criticare Technologies, Inc. |
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