Medical Device Recalls
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1 result found
510(K) Number: K070420 |
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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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| UroSeal Adjustable Endoscopic Valve. Model/Catalog # 00913410 The primary packaging is a Tyvek pou... | 2 | 12/23/2014 |
FEI # 1000122656 US Endoscopy Group Inc |
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