FDA 510(k) Applications Submitted by Aaron Ge

FDA 510(k) Number Submission Date Device Name Applicant
K152257 08/10/2015 Fujifilm Duodenoscope Model ED-530XT FUJIFILM MEDICAL SYSTEMS U.S.A., INC.
K153483 12/03/2015 Balloon controller PB-30 FUJIFILM MEDICAL SYSTEMS U.S.A., INC.
K170191 01/23/2017 SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision System MEDTRONIC VASCULAR, INC.


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