Bluezone Model RX-450 Air Purifier

FDA 510(k) K212824 · Bluezone Products, Inc.

Substantially Equivalent

510(k) numberK212824

Submission

Device name
Bluezone Model RX-450 Air Purifier
Applicant
Bluezone Products, Inc.
Woburn, MA, US
Received
September 3, 2021
Decision date
February 17, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FRA – Purifier, Air, Ultraviolet, Medical
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6500
Specialty
General Hospital

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Questions and answers

When was Bluezone Model RX-450 Air Purifier cleared by the FDA?

Bluezone Model RX-450 Air Purifier (K212824) received a 510(k) decision of Substantially Equivalent on February 17, 2022, 167 days after the submission was received.

What is the product code of K212824?

The FDA product code is FRA – Purifier, Air, Ultraviolet, Medical, a Class II (moderate risk) device regulated under 21 CFR 880.6500.