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Heidelberg Engineering

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K101223	SPECTRALIS HRA+OCT, SPECTRALIS FA_OCT, SPECTRALIS ICGA+ OCT, SPECTRALIS HRA, SPECTRALIS FA	OBO	2010-10-01	View
510(k)	K063191	HEIDELBERG RETINA ANGIOGRAPH 2/OPTICAL COHERENCE TOMOGRAPH, MODEL HRA 2/OCT	OBO	2006-10-31	View
510(k)	K052935	HEIDELBERG ENGINEERING SLITLAMP-OCT (SL-OCT)	MXK	2006-01-13	View
510(k)	K042742	HEIDELBERG RETINA TOMOGRAPH II / ROSTOCK CORNEA MODULE (HRT II / RCM)	MXK	2004-10-13	View
510(k)	K971671	HEIDELBERG RETINA ANGIOGRAPH FA/ICGA (HRA/C)	HLI	1997-07-29	View
510(k)	K943956	RETINA TOMOGRAPH AND FLOWMETER	HLI	1994-11-14	View
510(k)	K943955	RETINA FLOWMETER	HLI	1994-11-14	View
510(k)	K944261	RETINA ANGIOGRAPH	HLI	1994-11-14	View
510(k)	K912891	HEIDELBERG RETINA TOMOGRAPH	HLI	1991-09-27	View

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