FDA 510(k) Applications Submitted by JUDITH A BRIMACOMBE, MA

FDA 510(k) Number	Submission Date	Device Name	Applicant
K100468	02/18/2010	ZEISS INFRARED 800 WITH FLOW 800 OPTION	CARL ZEISS SURGICAL GMBH
K100035	01/06/2010	MODEL VISULAS 532S LASER WITH THE VITE OPTION	CARL ZEISS MEDITEC AG
K100253	01/28/2010	VISUMAX LASER KERATOME	CARL ZEISS MEDITEC AG
K111157	04/25/2011	CIRRUS HD-OCT WITH RETINAL NERVE FIBER LAYER, MACULAR, OPTIC NERVE HEAD, and GANGLION CELL NORMATIVE DATABASES	CARL ZEISS MEDITEC INC
K101182	04/27/2010	IOLMASTER 500	CARL ZEISS MEDITEC AG
K051789	07/01/2005	VISANTE OCT	CARL ZEISS MEDITEC INC
K082016	07/15/2008	GDX VCC WITH ECC SOFTWARE	CARL ZEISS MEDITEC INC.
K112184	07/28/2011	CIRRUS PHOTO	CARL ZEISS MEDITEC INC
K122418	08/08/2012	IOLMASTER 500	CARL ZEISS MEDITEC AG
K093213	10/13/2009	GUIDED PROGRESSION ANALYSIS ON THE HUMPHREY FIELD ANALYZER II AND II -I SERIES	CARL ZEISS MEDITEC INC
K103056	10/15/2010	VISULAS TRION LASER SYSTEM WITH THE VITE OPTION	CARL ZEISS MEDITEC AG
K083291	11/07/2008	CIRRUS HD-OCT WITH RETINAL NERVE FIBER LAYER AND MACULAR NORMATIVE DATABASES, MODEL 4000	CARL ZEISS MEDITEC INC
K063378	11/08/2006	CIRRUS HD-OCT, MODEL 4000	CARL ZEISS MEDITEC INC
K110590	03/02/2011	INTRABEAM NEEDLE APPLICATOR	CARL ZEISS SURGICAL GMBH
K182480	09/10/2018	Earlens Contact Hearing Aid	Earlens Corporation