Medical Device Recalls
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1 result found
510(K) Number: K182971 |
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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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| SpaceOAR Vue System, UPN SV-1010 and SV-2101. Used to temporarily position the anterior rectal wall... | 2 | 04/25/2022 |
FEI # 3005099803 Boston Scientific Corporation |
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