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INSTRUMENT,FILLING,PLASTIC,DENTAL

K945077 Class I Traditional
Decision Date
1994-11-30
Sponsor / Applicant
Worldwide Dental, Inc.

Technical Specification

510(k) Submission ID K945077
Product Code EKJ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1994-11-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INSTRUMENT,FILLING,PLASTIC,DENTAL received FDA 510(k) clearance under submission number K945077, sponsored by Worldwide Dental, 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 1994-11-30.

Classification & Regulation

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