Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K221925 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/Catalog Number: 192-... | 2 | 04/15/2025 | Abbott Diagnostics Scarborough, Inc. |
| Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/Catalog Number: 192-... | 2 | 04/15/2025 | Abbott Diagnostics Scarborough, Inc. |
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