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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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