Clearance Summary
SurBlate Ablation System received FDA 510(k) clearance under submission number K223272, sponsored by Mima-Pro Scientific, Inc.. 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 2023-02-28.
- Submission: K223272
- Applicant / Sponsor: Mima-Pro Scientific, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2023-02-28
Classification & Regulation
This clearance is catalogued under FDA product code NEY and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.