Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K910253 |
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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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CooperSurgical LEEP REDIKIT-Used as a surgical preparatory kit for Loop Electrosurgical Excision Pro... | 3 | 10/06/2015 | CooperSurgical, Inc. |
LEEP REDIKIT Product No. 6060 In a Loop Electrosurgical Excision Procedure, a thin, low-volt... | 2 | 04/03/2013 | Cooper Surgical, Inc. |
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