# K220298: CerroZone Mobile

- Pathway: 510(k) (Traditional)
- Applicant: Cerrozone
- Decided: Jul 1, 2022 after 149 days
- Product code: FRF (Cleaner, Air, Medical Recirculating)
- Device class: 2
- Regulation: 21 CFR 880.5045
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K972064 (1997). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K200321: Novaerus NV1050, Novaerus Us, Inc. (2020) Summary page 4.

## Most influential descendants
- K242102: CerroZone Mini (2024), 0 descendants of its own

## Indications for use
The CerroZone Mobile is intended as a room recirculating air cleaner. The system is used for filtering out and inactivating airborne particles (i.e., bacteria and viruses) from the air for medical purposes.

Source page: https://510kreport.com/device/K220298
Methodology: https://510kreport.com/methodology