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United States Endoscopy Group, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10
Categories6
Latest FDA decision2020-05-21
TypeNumberDevice NameCodeDateActions
510(k) K192265 gi-4000 Electrosurgical GeneratorGEI2020-05-21 View
510(k) K200745 Lariat, Hot/Cold SnareFDI2020-04-21 View
510(k) K192059 Bio Guard Air/Water & Suction ValvesODC2019-09-17 View
510(k) K191559 AquaShield System CO2, AquaShield System CO2-PENTAX, AquaShield System CO2-FUJIFILMFEQ2019-08-01 View
510(k) K182909 Roth Net Retriever Product LineFDI2018-11-21 View
510(k) K182258 AquaShield System CO2 ; AquaShield System CO2 - PENTAX ; AquaShield System CO2 - FujifilmFEQ2018-09-21 View
510(k) K173650 AquaShield System CO2- FujifilmFEQ2018-01-05 View
510(k) K172805 gi-4000 Electrosurgical GeneratorGEI2017-10-23 View
510(k) K163495 AdvanCE capsule endoscope delivery deviceNEZ2017-03-10 View
510(k) K163492 Oracle EUS Balloon; Oracle EUS latex balloon - Olympus Radial; Oracle EUS latex balloon - Olympus Linear; Oracle EUS latex balloon - Fujinon Radial; Oracle EUS latex balloon - Fujinon LinearFDF2017-01-06 View
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