meddevicedb.com FDA Device Reference

K-SPRAY, MODEL 085-2715

K062418 Class I Traditional
Decision Date
2006-10-19
Sponsor / Applicant
Scican

Technical Specification

510(k) Submission ID K062418
Product Code EFB
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2006-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

K-SPRAY, MODEL 085-2715 received FDA 510(k) clearance under submission number K062418, sponsored by Scican. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-10-19.

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.