Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K954797 |
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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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Broncho Flexible Fiberscope, models: 11001BN1, 11002BD1, 11004BC1, and 11009BC1. " Examination an... | 2 | 12/17/2013 | Karl Storz Endoscopy America Inc |
Karl Storz SE & CO. KG, REF 11003MB, Grasping Forceps, Flexible 1 mm, Rx Only | 2 | 04/03/2024 | Karl Storz Endoscopy |
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