Medical Device Recalls
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1 result found
510(K) Number: K092879 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Covidien, LigaSure, Blunt Tip Laparoscopic Sealer/Divider, 5 mm-37 cm, REF LF1537, Sterile EO, Covid... | 2 | 01/25/2011 | Covidien LP |
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