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SOFT DENTURE RELINE MATERIAL ELASTOLINE

K925275 Class II Traditional
Decision Date
1993-01-11
Sponsor / Applicant
Great Lakes Orthodontics, Ltd.

Technical Specification

510(k) Submission ID K925275
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 1993-01-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOFT DENTURE RELINE MATERIAL ELASTOLINE received FDA 510(k) clearance under submission number K925275, sponsored by Great Lakes Orthodontics, 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 1993-01-11.

Classification & Regulation

This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.