meddevicedb.com FDA Device Reference

Air Pressure Therapy System

K201935 Class II Traditional
Decision Date
2021-06-22
Sponsor / Applicant
Xiamen Weiyou Intelligent Technology Co., Ltd.

Technical Specification

510(k) Submission ID K201935
Product Code IRP
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5650
Decision Date 2021-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Air Pressure Therapy System received FDA 510(k) clearance under submission number K201935, sponsored by Xiamen Weiyou Intelligent Technology Co., Ltd.. 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 2021-06-22.

Classification & Regulation

This clearance is catalogued under FDA product code IRP and 21 CFR 890.5650, within the Physical Medicine review panel as a Class II device.