meddevicedb.com FDA Device Reference

Quickie(r) Q700-UP M

K172384 Class II Traditional
Decision Date
2018-01-16
Sponsor / Applicant
Sunrise Medical (Us), LLC

Technical Specification

510(k) Submission ID K172384
Product Code IPL
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3900
Decision Date 2018-01-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Quickie(r) Q700-UP M received FDA 510(k) clearance under submission number K172384, sponsored by Sunrise Medical (Us), LLC. 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 2018-01-16.

Classification & Regulation

This clearance is catalogued under FDA product code IPL and 21 CFR 890.3900, within the Physical Medicine review panel as a Class II device.