Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K012232 |
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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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| ZVU Functional GI Software, REF: ZVU-3 | 3 | 09/07/2023 |
FEI # 2023374 Diversatek Healthcare |
| Insight rev H software. The InSIGHT Gastrointestinal Motility System is intended for use by gast... | 2 | 05/07/2012 |
FEI # 2023374 Sandhill Scientific, Inc |
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