Medical Device Recalls
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1 result found
510(K) Number: K160455 |
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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 AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device (Intervent... | 2 | 04/10/2026 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
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