Medical Device Recalls
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1 result found
510(K) Number: K090807 |
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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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Nonin Model 7600B cerebral oximeter pod. Used with the Nonin Model 7600 Regional Oximeter with Equa... | 2 | 11/25/2009 | Nonin Medical, Inc |
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