Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K962925 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| B5-2C BALLOON CATHETER 11MM DIA 2.0; Model No. B5-2C - Product Usage: Used with endoscopes to inject... | 2 | 02/05/2021 |
FEI # 3003995201 Aomori Olympus Co., Ltd. |
| B5-2Q BALLOON CATHETER, Model No. B5-2Q - Product Usage: Used with endoscopes to inject contrast med... | 2 | 02/05/2021 |
FEI # 3003995201 Aomori Olympus Co., Ltd. |
| B7-2C BALLOON CATHETER 13mm dia 2.8; model no. B7-2C - Product Usage: Used with endoscopes to inject... | 2 | 02/05/2021 |
FEI # 3003995201 Aomori Olympus Co., Ltd. |
| B7-2LA BALLOON CATHETER 13MM DIA 3.2, model no. B7-2LA - Product Usage: Used with endoscopes for inj... | 2 | 02/05/2021 |
FEI # 3003995201 Aomori Olympus Co., Ltd. |
| B7-2Q BALLOON CATHETER 13MM DIA 3.2, model no. B7-2Q -Product Usage: Used with endoscopes for inject... | 2 | 02/05/2021 |
FEI # 3003995201 Aomori Olympus Co., Ltd. |
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