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INSTRUMENT, DENTAL

K834072 Class I Traditional
Decision Date
1984-02-21
Sponsor / Applicant
Venture Technology, Inc.

Technical Specification

510(k) Submission ID K834072
Product Code EMS
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1984-02-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INSTRUMENT, DENTAL received FDA 510(k) clearance under submission number K834072, sponsored by Venture Technology, 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 1984-02-21.

Classification & Regulation

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