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TRX POWER TILT AND RECLINE SYSTEM

K970521 Class II Traditional
Decision Date
1997-03-31
Sponsor / Applicant
Motion Concepts

Technical Specification

510(k) Submission ID K970521
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 1997-03-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRX POWER TILT AND RECLINE SYSTEM received FDA 510(k) clearance under submission number K970521, sponsored by Motion Concepts. 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 1997-03-31.

Classification & Regulation

This clearance is catalogued under FDA product code ITI and 21 CFR 890.3860, within the Physical Medicine review panel as a Class II device.