Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K151801 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Arc Endocuff Vision as follows: ARV110 ENDOCUFF-V M BLUE PK8, Part Number: E0420501; ARV120 ENDOC... | 2 | 09/03/2021 |
FEI # 2429304 Olympus Corporation of the Americas |
| Endocuff Vision: models ARV 110, 120, 130, 140 Intended Use: ENDOCUFF VISION is a device attached... | 2 | 04/16/2020 |
FEI # 3009837469 Boddingtons Plastics Ltd |
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