Medical Device Recalls
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510(K) Number: K112368 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| CAPNOSTREAM 20P (US) N, Part Number CS08651-01 | 2 | 10/03/2018 |
FEI # 3001227743 Oridion Medical 1987 Ltd. |
| CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-02 | 2 | 10/03/2018 |
FEI # 3001227743 Oridion Medical 1987 Ltd. |
| CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-03 | 2 | 10/03/2018 |
FEI # 3001227743 Oridion Medical 1987 Ltd. |
| CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-02 | 2 | 10/03/2018 |
FEI # 3001227743 Oridion Medical 1987 Ltd. |
| CAPNOSTREAM 20P (US) N W/PRINTER, Part Number CS08657-01 | 2 | 10/03/2018 |
FEI # 3001227743 Oridion Medical 1987 Ltd. |
| CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-03 | 2 | 10/03/2018 |
FEI # 3001227743 Oridion Medical 1987 Ltd. |
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