FDA 510(k) Applications Submitted by HEINE OPTOTECHNIK GMBH & CO. KG.

FDA 510(k) Number Submission Date Device Name Applicant
K123587 11/21/2012 HEINE MINI 3000 LED OPHTHALMOSCOPE HEINE OPTOTECHNIK GMBH & CO. KG.
K123316 10/25/2012 HEINE OMEGA 500 HEINE OPTOTECHNIK GMBH & CO. KG.
K131959 06/27/2013 HEINE MINI 3000(R) OPHTHALMOSCOPE HEINE OPTOTECHNIK GMBH & CO. KG.
K131961 06/27/2013 HEINE BETA 200(R) OPHTHALMOSCOPE HEINE OPTOTECHNIK GMBH & CO. KG.
K101892 07/07/2010 HEINE GAMMA G7; HEINE GAMMA G5, HEINE GAMMA GP, HEINE GAMMA GST, HEINE GAMMA XXL LF MODEL M-000.09.23X, M-000.09.24X, M- HEINE OPTOTECHNIK GMBH & CO. KG.


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