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