Clearance Summary
gi-4000 Electrosurgical Generator received FDA 510(k) clearance under submission number K172805, sponsored by United States Endoscopy Group, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2017-10-23.
- Submission: K172805
- Applicant / Sponsor: United States Endoscopy Group, Inc.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2017-10-23
Classification & Regulation
This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.