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BioSonic US200 Ultrasonic Scaler (60034537)

K240801 Class II Traditional
Decision Date
2024-07-01
Sponsor / Applicant
Dent4you AG

Technical Specification

510(k) Submission ID K240801
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 2024-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BioSonic US200 Ultrasonic Scaler (60034537) received FDA 510(k) clearance under submission number K240801, sponsored by Dent4you AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2024-07-01.

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.