meddevicedb.com FDA Device Reference

MIST IC

K222368 Class II Traditional
Decision Date
2022-12-01
Sponsor / Applicant
Imagine Milling Technologies, LLC

Technical Specification

510(k) Submission ID K222368
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2022-12-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MIST IC received FDA 510(k) clearance under submission number K222368, sponsored by Imagine Milling Technologies, 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 2022-12-01.

Classification & Regulation

This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.