Clearance Summary
GERSON 2130/31 TYPE N95 NIOSH CERTIFIED SURGICAL RESPIRATOR received FDA 510(k) clearance under submission number K050193, sponsored by Louis M. Gerson Co., 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 2005-04-11.
- Submission: K050193
- Applicant / Sponsor: Louis M. Gerson Co., Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4040
- Decision date: 2005-04-11
Classification & Regulation
This clearance is catalogued under FDA product code MSH and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.