# K951981: RXAIR 3000

- Pathway: 510(k) (Traditional)
- Applicant: Clean Air Research & Development
- Decided: Oct 12, 1995 after 168 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K133800: Odorox (R) Idu/RX (TM) in-Duct Models, Odorox (R) Idu/RX (TM) Mobile Disinfection Units, Odorox (R) Slimline/RX (TM) Slimli (2014), 1 descendant of its own
- K252128: Zener® (model ZEN-001-B1) (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K951981
Methodology: https://510kreport.com/methodology