Medical Device Recalls
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1 result found
510(K) Number: K091272 |
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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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Sunset Compressor Nebulizer, Model NEB100 - Product Usage: The Sunset Compressor Nebulizer is an AC-... | 2 | 03/26/2019 | SANRAI INTERNATIONAL LLC |
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