meddevicedb.com FDA Device Reference

K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT

K033263 Class II Traditional
Decision Date
2003-10-31
Sponsor / Applicant
Track Corporation

Technical Specification

510(k) Submission ID K033263
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2003-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT received FDA 510(k) clearance under submission number K033263, sponsored by Track Corporation. 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 2003-10-31.

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.