Medical Device Recalls
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1 result found
510(K) Number: K101889 |
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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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| Decompression Table Model E9011. This device applies cervical and/or lumbar decompression with pract... | 2 | 07/10/2024 |
FEI # 3007278668 Pivotal Health Solutions, Inc. |
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