meddevicedb.com FDA Device Reference

Kisses Mini

K170394 Class II Traditional
Decision Date
2017-10-06
Sponsor / Applicant
Achimhai Medical Corporation

Technical Specification

510(k) Submission ID K170394
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2017-10-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Kisses Mini received FDA 510(k) clearance under submission number K170394, sponsored by Achimhai Medical Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2017-10-06.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.