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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K141250
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VSE 11278... 2 05/12/2022 Karl Storz Endoscopy
11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VSE 11278... 2 05/12/2022 Karl Storz Endoscopy
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