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FDA 510(k) Applications Submitted by DAN W. LINDSAY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140382
02/14/2014
AEROMINI TRACHEOBRONCHIAL STENT TECHNOLOGY
MERIT MEDICAL SYSTEMS, INC.
K160107
01/19/2016
DiamondTOUCH Inflation Device and Fluid Dispensing Syringe
Merit Medical Systems, Inc.
K130566
03/04/2013
BASIXTOUCH
MERIT MEDICAL SYSTEMS, INC.
K102273
08/11/2010
MERIT BIPOLAR COAGULATION PROBE
MERIT MEDICAL SYSTEMS, INC.
K153672
12/21/2015
basixTOUCH40 Inflation Syringe
MERIT MEDICAL SYSTEMS, INC.
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