meddevicedb.com FDA Device Reference

Pressure Therapy System

K161907 Class II Traditional
Decision Date
2017-02-23
Sponsor / Applicant
Xiamen Senyang Co., Ltd.

Technical Specification

510(k) Submission ID K161907
Product Code IRP
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5650
Decision Date 2017-02-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Pressure Therapy System received FDA 510(k) clearance under submission number K161907, sponsored by Xiamen Senyang 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 2017-02-23.

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.