Clearance Summary
PERIO-FLOW nozzle received FDA 510(k) clearance under submission number K171174, sponsored by E.M.S Electro Medical Systems S.A. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2017-12-18.
- Submission: K171174
- Applicant / Sponsor: E.M.S Electro Medical Systems S.A
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 2017-12-18
Classification & Regulation
This clearance is catalogued under FDA product code EFB and 21 CFR 872.4200, within the Dental review panel as a Class I device.