meddevicedb.com FDA Device Reference

Airdog X8 Air Purifier (KJ800F-X8)

K240696 Class II Special
Decision Date
2024-06-14
Sponsor / Applicant
Suzhou Beiang Smart Technology Co., Ltd.

Technical Specification

510(k) Submission ID K240696
Product Code FRF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5045
Decision Date 2024-06-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Airdog X8 Air Purifier (KJ800F-X8) received FDA 510(k) clearance under submission number K240696, sponsored by Suzhou Beiang Smart Technology Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2024-06-14.

Classification & Regulation

This clearance is catalogued under FDA product code FRF and 21 CFR 880.5045, within the General Hospital review panel as a Class II device.