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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