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QUANTEC SERIES 2000 ENDODONTIC FILES

K962031 Class I Traditional
Decision Date
1996-06-04
Sponsor / Applicant
Tycom Dental

Technical Specification

510(k) Submission ID K962031
Product Code EKS
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1996-06-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUANTEC SERIES 2000 ENDODONTIC FILES received FDA 510(k) clearance under submission number K962031, sponsored by Tycom Dental. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1996-06-04.

Classification & Regulation

This clearance is catalogued under FDA product code EKS and 21 CFR 872.4565, within the Dental review panel as a Class I device.