meddevicedb.com FDA Device Reference

Manual Wheelchair (SYIV100A008)

K252517 Class I Traditional
Decision Date
2025-10-03
Sponsor / Applicant
Ningbo Shenyu Medical Equipment Co.,Ltd

Technical Specification

510(k) Submission ID K252517
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2025-10-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Manual Wheelchair (SYIV100A008) received FDA 510(k) clearance under submission number K252517, sponsored by Ningbo Shenyu Medical Equipment 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 2025-10-03.

Classification & Regulation

This clearance is catalogued under FDA product code IOR and 21 CFR 890.3850, within the Physical Medicine review panel as a Class I device.