Medical Device Recalls
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1 result found
510(K) Number: K020135 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Conmed System 2500 Electrosurgical Unit, REF 60-8011-SYS, Conmed Corporation | 2 | 09/19/2006 |
FEI # 3004491689 Conmed Electrosurgery |
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