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ULTRASONIC SCALER 3000/ PROPHY-JET 30/ CAVI-JET 30

K864996 Class II Traditional
Decision Date
1987-02-19
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K864996
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 1987-02-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRASONIC SCALER 3000/ PROPHY-JET 30/ CAVI-JET 30 received FDA 510(k) clearance under submission number K864996, sponsored by Dentsply Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1987-02-19.

Classification & Regulation

This clearance is catalogued under FDA product code ELC and 21 CFR 872.4850, within the Dental review panel as a Class II device.