Clearance Summary
DELTA N95 RESPIRATOR received FDA 510(k) clearance under submission number K964722, sponsored by Racal Filter Technologies, 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 1997-02-07.
- Submission: K964722
- Applicant / Sponsor: Racal Filter Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4040
- Decision date: 1997-02-07
Classification & Regulation
This clearance is catalogued under FDA product code FXX and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.