meddevicedb.com FDA Device Reference

SIMS CHAIR

K861632 Class II Traditional
Decision Date
1986-05-27
Sponsor / Applicant
Twin City Surgical, Inc.

Technical Specification

510(k) Submission ID K861632
Product Code IKK
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.1925
Decision Date 1986-05-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIMS CHAIR received FDA 510(k) clearance under submission number K861632, sponsored by Twin City Surgical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1986-05-27.

Classification & Regulation

This clearance is catalogued under FDA product code IKK and 21 CFR 890.1925, within the Physical Medicine review panel as a Class II device.