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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