FDA 510(k) Applications Submitted by LUCO HYBRID OSA APPLIANCE INC.

FDA 510(k) Number Submission Date Device Name Applicant
K160477 02/19/2016 The Luco Hybrid OSA Appliance LUCO HYBRID OSA APPLIANCE INC.
K130797 03/22/2013 LUCO HYBRID OSA APPLIANCE LUCO HYBRID OSA APPLIANCE INC.


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