meddevicedb.com FDA Device Reference

CHEMFIL

K812858 Class II Traditional
Decision Date
1981-12-31
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K812858
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 1981-12-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHEMFIL received FDA 510(k) clearance under submission number K812858, 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 1981-12-31.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.