meddevicedb.com FDA Device Reference

SNAPSHOT

K081925 Class II Traditional
Decision Date
2008-09-02
Sponsor / Applicant
Instrumentarium Dental, Palodex Group OY

Technical Specification

510(k) Submission ID K081925
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2008-09-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SNAPSHOT received FDA 510(k) clearance under submission number K081925, sponsored by Instrumentarium Dental, Palodex Group OY. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2008-09-02.

Classification & Regulation

This clearance is catalogued under FDA product code MUH and 21 CFR 872.1800, within the Dental review panel as a Class II device.