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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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