meddevicedb.com FDA Device Reference

Q50 MEDICAL TREADMILL

K862741 Class I Traditional
Decision Date
1986-07-29
Sponsor / Applicant
Quinton, Inc.

Technical Specification

510(k) Submission ID K862741
Product Code IOL
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5380
Decision Date 1986-07-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Q50 MEDICAL TREADMILL received FDA 510(k) clearance under submission number K862741, sponsored by Quinton, 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 1986-07-29.

Classification & Regulation

This clearance is catalogued under FDA product code IOL and 21 CFR 890.5380, within the Physical Medicine review panel as a Class I device.