Medical Device Recalls
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1 result found
510(K) Number: K884947 |
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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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T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient use, non-sterile p... | 2 | 02/10/2016 | Salter Labs |
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