Medical Device Recalls
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1 result found
510(K) Number: K991830 |
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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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| CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter, REF/Catalog Number CS-023, STERILE, Rx Only P... | 2 | 10/14/2016 |
FEI # 3001451571 ConMed Corporation |
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