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FDA 510(k) Applications Submitted by Ken Luco
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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