meddevicedb.com FDA Device Reference

Fill-Up!

K150218 Class II Traditional
Decision Date
2015-06-23
Sponsor / Applicant
Coltene/Whaledent AG

Technical Specification

510(k) Submission ID K150218
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2015-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Fill-Up! received FDA 510(k) clearance under submission number K150218, sponsored by Coltene/Whaledent AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-06-23.

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.