meddevicedb.com FDA Device Reference

STRAP EASE 400

K803063 Class II Traditional
Decision Date
1980-12-22
Sponsor / Applicant
Independent Transfer Equipment Co.

Technical Specification

510(k) Submission ID K803063
Product Code ILK
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5150
Decision Date 1980-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STRAP EASE 400 received FDA 510(k) clearance under submission number K803063, sponsored by Independent Transfer Equipment Co.. 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 1980-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code ILK and 21 CFR 890.5150, within the Physical Medicine review panel as a Class II device.