Medical Device Recalls
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1 result found
510(K) Number: K092461 |
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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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Velocity" Biopsy Valve, 25 units per box, Product Usage: The disposable Velocity biopsy valve i... | 2 | 07/01/2015 | US Endoscopy Group Inc |
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