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FINECUBE DENTAL CT

K063622 Class II Traditional
Decision Date
2007-02-08
Sponsor / Applicant
The Yoshida Dental Mfg. Co., Ltd.

Technical Specification

510(k) Submission ID K063622
Product Code OAS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2007-02-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FINECUBE DENTAL CT received FDA 510(k) clearance under submission number K063622, sponsored by The Yoshida Dental Mfg. Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2007-02-08.

Classification & Regulation

This clearance is catalogued under FDA product code OAS and 21 CFR 892.1750, within the Radiology review panel as a Class II device.