meddevicedb.com FDA Device Reference

PM 2000 AUTOMATIC PATIENT CHAIR

K781597 Class II Traditional
Decision Date
1978-09-27
Sponsor / Applicant
Time Motion System Co.

Technical Specification

510(k) Submission ID K781597
Product Code FFG
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1800
Decision Date 1978-09-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PM 2000 AUTOMATIC PATIENT CHAIR received FDA 510(k) clearance under submission number K781597, sponsored by Time Motion System Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1978-09-27.

Classification & Regulation

This clearance is catalogued under FDA product code FFG and 21 CFR 876.1800, within the Gastroenterology, Urology review panel as a Class II device.