Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K173721 |
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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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| daVinci XI Sureform 60 Reload, 60 mm black 6-Row 4.6 mm, Ref: 48360T-08 , UDI: 00886874113851, Rx o... | 2 | 05/05/2020 |
FEI # 3001675293 Intuitive Surgical, Inc. |
| daVinci XI Sureform 60 reload, 60 mm Green 6- Row, 4.6 mm, REF 48360G-08, UDI: 00886874113844, Rx O... | 2 | 05/05/2020 |
FEI # 3001675293 Intuitive Surgical, Inc. |
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