Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K002016 |
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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| System Name: 722044 INTEGRIS Allura 15-12 (biplane) 722030 Integris CV Cesar-Powerpack-Visub-Nicol 7... | 2 | 09/18/2024 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
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