Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K190898 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Sight OLO-E1/U1 Software and Operators Manual Software v2.56.1 Catalog #: 1 OLO-U1 Catalog #: 2... | 2 | 09/22/2021 |
FEI # 3016099075 SIGHT DIAGNOSTICS LTD |
| The Sight OLO device is a computer vision based platform for blood analysis. The platform combines ... | 2 | 04/21/2022 |
FEI # 3016099075 SIGHT DIAGNOSTICS LTD |
| Sight OLO, Automated Hematology Analyzer, Catalog No. OLO-U1 | 2 | 07/27/2022 |
FEI # 3016099075 SIGHT DIAGNOSTICS LTD |
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