Medical Device Recalls
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1 result found
510(K) Number: K962879 |
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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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NebuTech Nebulizer, Model number: Series 8660, 8960, 8961, 8966, 8984. Nebulizer used to generate ae... | 2 | 09/17/2015 | Salter Labs |
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