Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K142779 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Simpleware ScanIP medical software. For transfer of imaging information from a medical scanner to a... | 2 | 08/12/2021 |
FEI # 3011676026 Simpleware Product Group, SYNOPSYS NORTHERN EUROPE |
| Simpleware ScanIP software. For transfer of imaging information from a medical scanner to an output ... | 2 | 08/12/2021 |
FEI # 3011676026 Simpleware Product Group, SYNOPSYS NORTHERN EUROPE |
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