Medical Device Recalls
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1 result found
510(K) Number: K110287 |
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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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| Philips 5-Lead Set, Disposable, Bedside, AAMI Model # 989803173131 Product Usage: Philips Singl... | 2 | 09/09/2019 |
FEI # 1218950 Philips North America, LLC |
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