Medical Device Recalls
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1 result found
510(K) Number: K012891 |
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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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Nellcor brand OxiMax Pulse Oximeter, model number N-595 Made in Ireland; Distributed by Tyco Heal... | 2 | 03/30/2005 | Nellcor Puritan Bennett |
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