Medical Device Recalls
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1 result found
510(K) Number: K113653 |
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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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EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80, iM50, M50, iM70, iM60, iM8, iM8A, iM8B Patie... | 2 | 10/11/2018 | Edan Diagnostics |
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