United States Endoscopy Group, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
Total Devices10
Categories6
Latest Approval2020-05-21
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K192265 | gi-4000 Electrosurgical Generator | GEI | 2020-05-21 | View |
| 510(k) | K200745 | Lariat, Hot/Cold Snare | FDI | 2020-04-21 | View |
| 510(k) | K192059 | Bio Guard Air/Water & Suction Valves | ODC | 2019-09-17 | View |
| 510(k) | K191559 | AquaShield System CO2, AquaShield System CO2-PENTAX, AquaShield System CO2-FUJIFILM | FEQ | 2019-08-01 | View |
| 510(k) | K182909 | Roth Net Retriever Product Line | FDI | 2018-11-21 | View |
| 510(k) | K182258 | AquaShield System CO2 ; AquaShield System CO2 - PENTAX ; AquaShield System CO2 - Fujifilm | FEQ | 2018-09-21 | View |
| 510(k) | K173650 | AquaShield System CO2- Fujifilm | FEQ | 2018-01-05 | View |
| 510(k) | K172805 | gi-4000 Electrosurgical Generator | GEI | 2017-10-23 | View |
| 510(k) | K163495 | AdvanCE capsule endoscope delivery device | NEZ | 2017-03-10 | 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 Linear | FDF | 2017-01-06 | View |
No matching devices.