Medical Device Recalls
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1 result found
510(K) Number: K944400 |
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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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Pedi-Cap CO2 Detector, 1 kg - 15 kg, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Ple... | 1 | 09/08/2009 | Covidien Limited |
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