# K242102: CerroZone Mini

- Pathway: 510(k) (Traditional)
- Applicant: Cerrozone, LLC
- Decided: Nov 19, 2024 after 124 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: 4 generations back to K972064 (1997). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K220298: CerroZone Mobile, Cerrozone (2022) Summary page 5.

## Indications for use
The CerroZone Mini 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/K242102
Methodology: https://510kreport.com/methodology