meddevicedb.com FDA Device Reference

Oxygen Concentrator

K202389 Class II Traditional
Decision Date
2022-04-08
Sponsor / Applicant
Foshan Mic Medical Technology Co., Ltd.

Technical Specification

510(k) Submission ID K202389
Product Code CAW
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5440
Decision Date 2022-04-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Oxygen Concentrator received FDA 510(k) clearance under submission number K202389, sponsored by Foshan Mic Medical Technology 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 2022-04-08.

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.