# K902120: Mercury Rhinomanometer

- Pathway: 510(k) (Traditional)
- Applicant: Life-Tech Intl., Inc.
- Decided: Aug 6, 1990 after 87 days
- Product code: BXQ (Rhinoanemometer (Measurement Of Nasal Decongestion))
- Device class: 2
- Regulation: 21 CFR 868.1800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K022311: Rhinostream Rhinomanometer Module (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K902120
Methodology: https://510kreport.com/methodology