FDA 510(k) Applications Submitted by MICHAEL O'SULLIVAN

FDA 510(k) Number Submission Date Device Name Applicant
K141295 05/19/2014 MERIT HYDROPHILIC GUIDEWIRE MERIT MEDICAL SYSTEMS, INC.
K142051 07/28/2014 PRELUDE PLASTIC JACKETED GUIDE WIRE MERIT MEDICAL SYSTEMS INC.
K052969 10/21/2005 SLENDERTONE GYMBODY, MODEL 512-01 BIO-MEDICAL RESEARCH, LTD.


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