Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K933200 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PBD-203-0703 BILIARY STENT, model no. PBD-203-0703 - Product Usage: Used with endoscopes for endosco... | 2 | 02/05/2021 |
FEI # 3003995201 Aomori Olympus Co., Ltd. |
| PBD-203-0710 BILIARY STENT, model no. PBD-203-0710 -Product Usage: Used with endoscopes for endoscop... | 2 | 02/05/2021 |
FEI # 3003995201 Aomori Olympus Co., Ltd. |
| PBD-203-0707 BILIARY STENT, model no. PBD-203-0707 -Product Usage: Used with endoscopes for endoscop... | 2 | 02/05/2021 |
FEI # 3003995201 Aomori Olympus Co., Ltd. |
| PBD-203-0704 BILIARY STENT, model no. PBD-203-0704 -Product Usage: Used with endoscopes for endoscop... | 2 | 02/05/2021 |
FEI # 3003995201 Aomori Olympus Co., Ltd. |
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