Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K201770 |
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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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Masimo Rad-G, Pulse Oximeter (W/Patient Cable), REF:9849, Rx Only, | 2 | 04/12/2024 | Masimo Corporation |
Masimo Rad-G, Pulse Oximeter (W/Sensor), REF:9847, Rx Only, | 2 | 04/12/2024 | Masimo Corporation |
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