Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K151859 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The Synapse Cardiovascular i... | 2 | 06/02/2021 | Fujifilm Medical Systems U.S.A., Inc. |
| Synapse CV 6. with AR. A web-based application as the primary user interface for the processing o... | 2 | 02/21/2024 | FUJIFILM Healthcare Americas Corporation |
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