Clearance Summary
PREMIER NITROSPRAY PLUS AND PREMIER NITROSPRAY LITE PLUS received FDA 510(k) clearance under submission number K970992, sponsored by Premier Dental Products Co.. 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 1997-06-17.
- Submission: K970992
- Applicant / Sponsor: Premier Dental Products Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4350
- Decision date: 1997-06-17
Classification & Regulation
This clearance is catalogued under FDA product code GEH and 21 CFR 878.4350, within the General, Plastic Surgery review panel as a Class II device.