Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K911098 |
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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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UroDiagnost Eleva, system code 708033 | 2 | 03/13/2020 | Philips North America, LLC |
Urodiagnost, Product No. 708033 Product Usage: The Philips UroDiagnost MRF can be used to perfor... | 2 | 03/23/2019 | Philips North America, LLC |
708033 URODiagnost As a multifunctional universal imaging application system, General RJF, Fluoro... | 2 | 05/03/2018 | Philips Medical Systems Nederlands |
UroDiagnost; x-ray system. Product Code: 708033 | 2 | 08/01/2016 | Philips Electronics North America Corporation |
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