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ORTHODONTIC ELASTICS

K810010 Class I Traditional
Decision Date
1981-01-28
Sponsor / Applicant
Orec Corp.

Technical Specification

510(k) Submission ID K810010
Product Code ECI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5410
Decision Date 1981-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHODONTIC ELASTICS received FDA 510(k) clearance under submission number K810010, sponsored by Orec Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1981-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code ECI and 21 CFR 872.5410, within the Dental review panel as a Class I device.