Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K112368 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CAPNOSTREAM 20P (US) N, Part Number CS08651-01 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-02 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-03 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-02 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
CAPNOSTREAM 20P (US) N W/PRINTER, Part Number CS08657-01 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-03 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
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