Clearance Summary
ProGear® Surgical Mask with Oxafence®, Model AV82030 received FDA 510(k) clearance under submission number K231741, sponsored by Prestige Ameritech. 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 2024-09-05.
- Submission: K231741
- Applicant / Sponsor: Prestige Ameritech
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4040
- Decision date: 2024-09-05
Classification & Regulation
This clearance is catalogued under FDA product code OUK and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.