Medical Device Recalls
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1 result found
510(K) Number: K945185 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| CYSTO-URETHRO-FIBERSCOPE REF 11272C1 CYSTOSCOPE, 15FR X 370MM, ADULT REF 11272C2 and Kit Number ... | 2 | 05/12/2022 | Karl Storz Endoscopy |
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