Medical Device Recalls
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1 result found
510(K) Number: K914008 |
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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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Cystoscope Intended to provide optical visualization of and therapeutic access to the Urinary Tract... | 2 | 06/28/2016 | Pentax Medical Company |
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