FDA 510(k) Applications Submitted by Lutech Industries, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K170446 02/14/2017 LT-300 SD Digital Video Colposcope Lutech Industries, Inc.
K143119 10/30/2014 LT-300 Video Colposcope Lutech Industries, Inc.
K160380 02/10/2016 LT-300 HD Lutech Industries, Inc.
K150691 03/18/2015 Datalys Multi-Parameter Patient Monitor Lutech Industries, Inc.


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