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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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