Medical Device Recalls
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1 result found
510(K) Number: K142107 |
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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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TRUE 3D VIEWER SYSTEM Model Number EP-00001-XX Software versions 1.0, 1.25, and 1.35 The t3D-V... | 2 | 05/21/2025 | Echopixel, Inc. |
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