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FDA 510(k) Applications Submitted by HEINE Optotechnik GmbH & Co. KG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K142486
09/04/2014
HEINE BETA 200, HEINE BETA 200 S, HEINE K 180
HEINE Optotechnik GmbH & Co. KG
K142837
09/30/2014
HEINE SIGMA 250 & HEINE SIGMA 250 M2
HEINE Optotechnik GmbH & Co. KG
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