meddevicedb.com FDA Device Reference

MUSTANG

K954376 Class I Traditional
Decision Date
1995-12-08
Sponsor / Applicant
Temco, Inc.

Technical Specification

510(k) Submission ID K954376
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 1995-12-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MUSTANG received FDA 510(k) clearance under submission number K954376, sponsored by Temco, 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 1995-12-08.

Classification & Regulation

This clearance is catalogued under FDA product code IOR and 21 CFR 890.3850, within the Physical Medicine review panel as a Class I device.