# K241202: Electric nasal aspirator (HTD2601US)

- Pathway: 510(k) (Traditional)
- Applicant: Hetaida Technology Co., Ltd.
- Decided: Jul 1, 2024 after 62 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
Longest line of descent: 7 generations back to K935218 (1994). 9 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K222547: Electric nasal aspirator, Shenzhen Xinlianfeng Technology Co.,Ltd (2022) Summary page 4.

## Most influential descendants
- K260473: Electric nasal aspirator (BC027, BC030, BC033, BC035, BC035B) (2026), 0 descendants of its own

## Indications for use
The Electronic Nasal Aspirator is intended for intermittent removal of nasal secretions and mucus from children (age 2-12 years old). This device is used in a home environment.

Source page: https://510kreport.com/device/K241202
Methodology: https://510kreport.com/methodology