Medical Device Recalls
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1 result found
510(K) Number: K980299 |
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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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GE ApexPro Oximeter systems (ApexPro CH or ApexPro FH with ApexPro Telemetry version 3.9 software) | 2 | 01/13/2010 | General Electric Medical Systems Information Technology |
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