# K023830: Airocide TI02

- Pathway: 510(k) (Traditional)
- Applicant: Kes Science & Technology, Inc.
- Decided: Feb 4, 2003 after 78 days
- Product code: FRA (Purifier, Air, Ultraviolet, Medical)
- Device class: 2
- Regulation: 21 CFR 880.6500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
17 later devices descend from it; 2 cite it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K033448: Electro-Optical Air Sterilizer with Ionizer (2004), 16 descendants of its own
- K052732: Abracair Air Cleaner, Model QTZ300-60; Abracair Air Cleaner, Model TI 100-30P (2006), 15 descendants of its own
- K161468: Transformair Indoor Air Purifier (2017), 14 descendants of its own
- K200500: Molekule Air Pro RX (2020), 11 descendants of its own
- K202339: Molekule Air Mini, Molekule Air Mini + (2021), 9 descendants of its own

## Indications for use
AiroCide Ti02 INTENDED USE: Potential applications include removing and mineralizing airborne contaminations of pathogens and/or harmful molds and volatile organic compounds present in rooms or enclosed areas: treatment rooms, hospital wards, intensive care hospital wards, hulding areas in jails, operating rooms, homeless shelters, pediatric waiting areas, command and control vehicles, embalming rooms in funeral homes, postal facilities. etc

Source page: https://510kreport.com/device/K023830
Methodology: https://510kreport.com/methodology