Medical Device Recalls
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1 result found
510(K) Number: K033296 |
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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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| Masimo LNOP TC-I SpO2, Reusable Ear Sensor, REF: 1794 | 2 | 06/21/2023 |
FEI # 3011353843 Masimo Corporation |
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