Medical Device Recalls
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1 result found
510(K) Number: K133175 |
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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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| Draeger Jaundice Meter JM-105 The device is intended for use in hospitals, clinics or doctor s of... | 1 | 06/07/2018 |
FEI # 2510954 Draeger Medical Systems, Inc. |
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