Medical Device Recalls
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1 result found
510(K) Number: K100403 |
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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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Masimo Hemoglobin Pronto-7 with Rainbow 40 Technology for easy-to-use spot-check testing of hemogl... | 2 | 02/22/2011 | Masimo Corporation |
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