Airdog X8 Air Purifier (KJ800F-X8)

FDA 510(k) K240696 · Suzhou Beiang Smart Technology Co., Ltd.

Substantially Equivalent

510(k) numberK240696

Submission

Device name
Airdog X8 Air Purifier (KJ800F-X8)
Applicant
Suzhou Beiang Smart Technology Co., Ltd.
Suzhou, CN
Received
March 14, 2024
Decision date
June 14, 2024
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FRF – Cleaner, Air, Medical Recirculating
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5045
Specialty
General Hospital

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K200321Novaerus NV1050FRF · Traditional Novaerus Us, Inc.12/28/2020SE
K130702Airsonett AIR-4FRF · Traditional Airsonett AB07/23/2013SE
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Questions and answers

When was Airdog X8 Air Purifier (KJ800F-X8) cleared by the FDA?

Airdog X8 Air Purifier (KJ800F-X8) (K240696) received a 510(k) decision of Substantially Equivalent on June 14, 2024, 92 days after the submission was received.

What is the product code of K240696?

The FDA product code is FRF – Cleaner, Air, Medical Recirculating, a Class II (moderate risk) device regulated under 21 CFR 880.5045.