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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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