# K220126: Geonic Nasal Aspirator, Geonic Nasal Cleaner

- Pathway: 510(k) (Traditional)
- Applicant: Geon Corporation
- Decided: Feb 2, 2023 after 380 days
- Product code: BTA (Pump, Portable, Aspiration (Manual Or Powered))
- Device class: 2
- Regulation: 21 CFR 878.4780
- 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’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K243138: Geon (S2) Nasal Aspirator (2025), 1 descendant of its own
- K253629: Momcozy Nasal Aspirator (BN007) (2026), 0 descendants of its own

## Indications for use
Geonic Nasal Aspirator (Model Name: AH2, S1) and Geonic Nasal Cleaner (Model Name: H2) are hand-held, non-invasive, electronic medical devices that provide negative pressure to remove nasal secretions and mucus from children (age 2-12 years old). Geonic Nasal Cleaner (Model Name: H2) additionally provide positive pressure to moisturize the nasal cavities by using saline solution in the form of spray for adults and pediatrics (3 years old). The nasal aspirator and nasal cleaner are intended for over-the-counter (OTC) use at home environment.

Source page: https://510kreport.com/device/K220126
Methodology: https://510kreport.com/methodology