meddevicedb.com FDA Device Reference

STREET

K032765 Class II Traditional
Decision Date
2004-01-30
Sponsor / Applicant
Permobil AB

Technical Specification

510(k) Submission ID K032765
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2004-01-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STREET received FDA 510(k) clearance under submission number K032765, sponsored by Permobil AB. 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 2004-01-30.

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.