meddevicedb.com FDA Device Reference

SPLATRFREE SWANGLE 360 DISPOSABLE PROPHYLAXIS ANGLE

K023232 Class I Traditional
Decision Date
2002-12-11
Sponsor / Applicant
Smartpractice

Technical Specification

510(k) Submission ID K023232
Product Code EFS
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6510
Decision Date 2002-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPLATRFREE SWANGLE 360 DISPOSABLE PROPHYLAXIS ANGLE received FDA 510(k) clearance under submission number K023232, sponsored by Smartpractice. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-12-11.

Classification & Regulation

This clearance is catalogued under FDA product code EFS and 21 CFR 872.6510, within the Dental review panel as a Class I device.