Medical Device Recalls
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1 result found
510(K) Number: K233810 |
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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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| Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection... | 2 | 11/07/2025 |
FEI # 3002806783 GE Healthcare Finland Oy |
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