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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K911808
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Accurus 2500 Standalone Vitreous Probe REF 8065741018; Accurus 23 GA Standalone Vitreous Probe REF 8... 2 06/29/2015 FEI # 1610287
Alcon Research, Ltd.
Alcon 25 GA Total Plus Pak, Catalog/Item #8065750220; for use with ACCURUS Vitrectomy System; distri... 2 05/26/2009 FEI # 1610287
Alcon Laboratories, Inc
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