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NICKEL-TITANIUM K-TYPE FILE

K935542 Class I Traditional
Decision Date
1994-01-03
Sponsor / Applicant
Union Broach, Div. Moyco Industries, Inc.

Technical Specification

510(k) Submission ID K935542
Product Code EKS
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1994-01-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NICKEL-TITANIUM K-TYPE FILE received FDA 510(k) clearance under submission number K935542, sponsored by Union Broach, Div. Moyco Industries, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1994-01-03.

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.