Medical Device Recalls
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1 result found
510(K) Number: K993979 |
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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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Model 509M Pulse Oximetry Interface Module Software versions 2.0 or 2.5 | 2 | 07/20/2004 | Respironics Novametrix, Inc. |
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