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DENTSPLY CAVITRON SPS SCALER SYSTEM

K970123 Class II Traditional
Decision Date
1997-04-11
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K970123
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 1997-04-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DENTSPLY CAVITRON SPS SCALER SYSTEM received FDA 510(k) clearance under submission number K970123, 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 1997-04-11.

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.