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FLUID-FILLED TEETHER

K092910 Class II Traditional
Decision Date
2009-12-18
Sponsor / Applicant
Qualiman Industrial Co., Ltd.

Technical Specification

510(k) Submission ID K092910
Product Code KKO
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5550
Decision Date 2009-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLUID-FILLED TEETHER received FDA 510(k) clearance under submission number K092910, sponsored by Qualiman Industrial Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-12-18.

Classification & Regulation

This clearance is catalogued under FDA product code KKO and 21 CFR 872.5550, within the Dental review panel as a Class II device.