Clearance Summary
Green OR Reprocessed Aquamantys Bipolar Sealer received FDA 510(k) clearance under submission number K211203, sponsored by Green Or, LLC. 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 2022-04-07.
- Submission: K211203
- Applicant / Sponsor: Green Or, LLC
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2022-04-07
Classification & Regulation
This clearance is catalogued under FDA product code NUJ and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.