meddevicedb.com FDA Device Reference

PROPHY CARE PASTE

K863133 Class I Traditional
Decision Date
1986-09-25
Sponsor / Applicant
Imd, Inc.

Technical Specification

510(k) Submission ID K863133
Product Code EJR
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6030
Decision Date 1986-09-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROPHY CARE PASTE received FDA 510(k) clearance under submission number K863133, sponsored by Imd, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1986-09-25.

Classification & Regulation

This clearance is catalogued under FDA product code EJR and 21 CFR 872.6030, within the Dental review panel as a Class I device.