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PLASTIC CHAIN

K925012 Class I Traditional
Decision Date
1993-09-13
Sponsor / Applicant
American Orthodontics

Technical Specification

510(k) Submission ID K925012
Product Code EJF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5410
Decision Date 1993-09-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLASTIC CHAIN received FDA 510(k) clearance under submission number K925012, sponsored by American Orthodontics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1993-09-13.

Classification & Regulation

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