Medical Device Recalls
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1 result found
510(K) Number: K982542 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Stryker Ureteral Kit, Model number 220-180-516, The ureteral kit is a ureteral transillumination dev... | 2 | 09/16/2008 |
FEI # 2936485 Stryker Endoscopy |
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