Clearance Summary
OKLand Patient Return Electrode Pad received FDA 510(k) clearance under submission number K183148, sponsored by Auckland Medical Polymer(Tianjin) Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2020-02-04.
- Submission: K183148
- Applicant / Sponsor: Auckland Medical Polymer(Tianjin) Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2020-02-04
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.