Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K062584 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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The Sophysa Pressio® Ventricular Intracranial Pressure Monitoring Kit monitoring is intended for mon... | 2 | 05/15/2024 | Sophysa S.A. |
The Sophysa Pressio® Ventricular Intracranial Pressure Monitoring Kit monitoring is intended for mon... | 2 | 05/15/2024 | Sophysa S.A. |
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