meddevicedb.com FDA Device Reference

PLAQUE-SWEEP

K873209 Class I Traditional
Decision Date
1987-08-25
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K873209
Product Code EFB
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 1987-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLAQUE-SWEEP received FDA 510(k) clearance under submission number K873209, 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 1987-08-25.

Classification & Regulation

This clearance is catalogued under FDA product code EFB and 21 CFR 872.4200, within the Dental review panel as a Class I device.