Medical Device Recalls
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1 result found
510(K) Number: K052859 |
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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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| Aquamantys 2.3 Bipolar Sealer Model #23-113-1. Product Usage: The Aquamantys Bipolar Sealer is a... | 2 | 07/28/2011 | Salient Surgical Technologies, Inc |
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