meddevicedb.com FDA Device Reference

DENTAL CHAIR F1

K884830 Class I Traditional
Decision Date
1989-02-10
Sponsor / Applicant
Fimet OY

Technical Specification

510(k) Submission ID K884830
Product Code KLC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6250
Decision Date 1989-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DENTAL CHAIR F1 received FDA 510(k) clearance under submission number K884830, sponsored by Fimet OY. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1989-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code KLC and 21 CFR 872.6250, within the Dental review panel as a Class I device.