meddevicedb.com FDA Device Reference

ORTHO PATIENT CHAIR

K884304 Class I Traditional
Decision Date
1989-04-25
Sponsor / Applicant
Halton Furniture Mfg.

Technical Specification

510(k) Submission ID K884304
Product Code KLC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6250
Decision Date 1989-04-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHO PATIENT CHAIR received FDA 510(k) clearance under submission number K884304, sponsored by Halton Furniture Mfg.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1989-04-25.

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.