Medical Device Recalls
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1 result found
510(K) Number: K181695 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Nihon Kohden NKV-550 Ventilator, REF: NKV-550-U, CE 0344, UDI: (01) 00843685100012 The Nihon Kohden... | 2 | 09/08/2021 |
FEI # 3014631252 NIHON KOHDEN ORANGEMED, INC |
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