Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K131818 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: M3 Product Description: ... | 2 | 01/22/2026 |
FEI # 3009499478 Edan Diagnostics |
| Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: M3A Product Description:... | 2 | 01/22/2026 |
FEI # 3009499478 Edan Diagnostics |
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