FDA 510(k) Applications Submitted by GERHARD ZINSER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K971671	05/07/1997	HEIDELBERG RETINA ANGIOGRAPH FA/ICGA (HRA/C)	HEIDELBERG ENGINEERING
K152205	08/06/2015	Spectralis HRA + OCT and variants (e.g.s below), Spectralis FA+OCT, Spectralis ICGA+OCT, Spectralis OCT Blue Peak, Spectralis OCT ith Multicolor	Heidelberg Engineering GmbH
K172649	09/05/2017	Spectralis HRA + OCT and variants, Spectralis FA+OCT, Spectralis ICGA+OCT, Spectralis OCT Blue Peak, Spectralis OCT with Multicolor	Heidelberg Engineering GmbH
K042742	10/04/2004	HEIDELBERG RETINA TOMOGRAPH II / ROSTOCK CORNEA MODULE (HRT II / RCM)	HEIDELBERG ENGINEERING
K052935	10/19/2005	HEIDELBERG ENGINEERING SLITLAMP-OCT (SL-OCT)	HEIDELBERG ENGINEERING
K063191	10/20/2006	HEIDELBERG RETINA ANGIOGRAPH 2/OPTICAL COHERENCE TOMOGRAPH, MODEL HRA 2/OCT	HEIDELBERG ENGINEERING
K113129	10/24/2011	SPECTRALIS ANTERIOR SEGMENT MODULE (SPECTRALIS ASM)	HEIDELBERG ENGINEERING GMBH