meddevicedb.com FDA Device Reference

CS 7600

K111649 Class II Traditional
Decision Date
2011-09-23
Sponsor / Applicant
Carestream Health, Inc.

Technical Specification

510(k) Submission ID K111649
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2011-09-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CS 7600 received FDA 510(k) clearance under submission number K111649, sponsored by Carestream Health, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2011-09-23.

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.