Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K091495 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| B-V233P-A 3-LUMEN EXTRACTION BALLOON V, model no. B-V233P-A - Product Usage: Used with endoscopes to... | 2 | 02/05/2021 |
FEI # 3003995201 Aomori Olympus Co., Ltd. |
| B-V443Q-A 3-LUMEN EXTRACTION BALLOON V, model no. B-V443Q-A - Product Usage: Used with endoscopes to... | 2 | 02/05/2021 |
FEI # 3003995201 Aomori Olympus Co., Ltd. |
| B-V243Q-A 3-LUMEN EXTRACTION BALLOON V, model no. B-V243Q-A - Product Usage: Used with endoscopes to... | 2 | 02/05/2021 |
FEI # 3003995201 Aomori Olympus Co., Ltd. |
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