Medical Device Recalls
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1 result found
510(K) Number: K230796 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Sparrow Ascent Patient Controller, REF's: 11-110-K, 11-310-K, 11-320-K, 11-321-K, 11-310-K-28, 11-32... | 2 | 08/11/2025 | Spark Biomedical Inc |
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