FDA 510(k) Applications Submitted by LENA SATTLER

FDA 510(k) Number Submission Date Device Name Applicant
K070836 03/27/2007 EXICLIP EXCS-M CLEVEX INC.
K121622 06/01/2012 NIDEK RS-3000 NIDEK CO., LTD.
K132323 07/25/2013 RS-3000 ADVANCE NIDEK CO., LTD.
K082891 09/30/2008 LENSTAR, MODEL LS900 HAAG-STREIT AG


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