Medical Device Recalls
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1 result found
510(K) Number: K081565 |
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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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Integre Pro Yellow LP561, Integre Pro Yellow LP6RY, Integre Pro Scan Green LP6G, Integre Pro Green L... | 2 | 06/27/2023 | Ellex Medical Pty Ltd. |
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