Medical Device Recalls
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1 result found
510(K) Number: K032403 |
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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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Oximeter Patient Cable Masimo 8 ft model number H5870. Filter, mask, and/or accessories for sleep ... | 2 | 04/24/2008 | Respironics, Inc. |
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