Medical Device Recalls
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1 result found
510(K) Number: K971198 |
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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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Babytherm 8004/8010, Infant Warmer, Class II device, 510 K K971198, Catalog # FR00105 (Babytherm 801... | 2 | 07/28/2016 | Draeger Medical, Inc. |
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