Medical Device Recalls
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1 result found
510(K) Number: K020524 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PatientNet Monitoring System - PatientNet Central Stations utilizing software Versions 1.03.14, 1.0... | 2 | 07/20/2004 |
FEI # 2124823 General Electric Medical Systems Information Technology |
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