meddevicedb.com FDA Device Reference

Oxygen Concentrator (J5A)

K251607 Class II Traditional
Decision Date
2025-11-21
Sponsor / Applicant
Foshan Kycare Medical Equipment Co., Ltd.

Technical Specification

510(k) Submission ID K251607
Product Code CAW
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5440
Decision Date 2025-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Oxygen Concentrator (J5A) received FDA 510(k) clearance under submission number K251607, sponsored by Foshan Kycare Medical Equipment Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2025-11-21.

Classification & Regulation

This clearance is catalogued under FDA product code CAW and 21 CFR 868.5440, within the Anesthesiology review panel as a Class II device.