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FDA 510(k) Applications Submitted by CARL ZEISS MEDITEC, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K161194
04/27/2016
PLEX Elite 9000 SS-OCT
CARL ZEISS MEDITEC, INC.
K143275
11/14/2014
IOLMaster700
Carl Zeiss Meditec, Inc.
K090439
02/20/2009
FORUM
CARL ZEISS MEDITEC, INC.
K181534
06/11/2018
CIRRUS HD-OCT
Carl Zeiss Meditec, Inc.
K121653
06/05/2012
INTRABEAM SYSTEM WITH INTRABEAM SPHERICAL APPLICATORS
CARL ZEISS MEDITEC, INC.
K181444
06/01/2018
CLARUS
Carl Zeiss Meditec, Inc.
K173371
10/27/2017
VisuMax Femtosecond Laser
Carl Zeiss Meditec, Inc.
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