Medical Device Recalls
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1 result found
510(K) Number: K180046 |
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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 RD Set TC-I SpO2 Adult Reusable Ear Sensor, REF: 4053 | 2 | 06/21/2023 | Masimo Corporation |
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