Clearance Summary
SPECTRASHIELD 9500 SURGICAL N95 RESPIRATOR received FDA 510(k) clearance under submission number K120244, sponsored by Nexera Medical, 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 2012-07-05.
- Submission: K120244
- Applicant / Sponsor: Nexera Medical, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4040
- Decision date: 2012-07-05
Classification & Regulation
This clearance is catalogued under FDA product code ONT and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.