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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K161194
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The PLEX Elite 9000, a Swept-Source OCT [SS-OCT] - Product Usage: The PLEX Elite 9000 Swept-Source ... 2 01/02/2020 FEI # 2918630
Carl Zeiss Meditec, Inc.
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