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FDA 510(k) Applications Submitted by United States Endoscopy Group, Inc
FDA 510(k) Number
Submission Date
Device Name
Applicant
K191559
06/13/2019
AquaShield System CO2, AquaShield System CO2-PENTAX, AquaShield System CO2-FUJIFILM
United States Endoscopy Group, Inc
K152035
07/22/2015
iSnare system-Lariat
United States Endoscopy Group, Inc
K192265
08/21/2019
gi-4000 Electrosurgical Generator
United States Endoscopy Group, Inc
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