Clearance Summary
Nuance FLOW received FDA 510(k) clearance under submission number K143679, sponsored by Den-Mat Holdings, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-05-01.
- Submission: K143679
- Applicant / Sponsor: Den-Mat Holdings, LLC
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3690
- Decision date: 2015-05-01
Classification & Regulation
This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.