Medical Device Recalls
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1 result found
510(K) Number: K042601 |
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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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Evaluation Kit, Capnostat 5, Respironics/Philips Product. Intended use of the Capnostat 5 CO2 sen... | 2 | 04/08/2010 | Philips Healthcare Inc. |
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