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U.S. Department of Health and Human Services

Medical Device Recalls

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1 result found
510(K) Number: K171402
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0 (10-2018) 2 05/10/2022 Karl Storz Endoscopy
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