Electric Nasal Aspirator (BC026, BC025, BC023, BC028, BC029, BC036)
by Shenzhen Kingboom Technology Co., Ltd.
510(k) K260147
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK260147 | Date13 Mar 2026 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- BTA
- Device Class
- Class II
- Regulation
- 21 CFR Part 878.4780
- Advisory Committee
- General, Plastic Surgery
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 22 Sep 2026
The Electric Nasal Aspirator is a portable pump device designed for aspiration. It is intended for use in medical settings to remove nasal secretions. The device is available in multiple model numbers including BC026, BC025, BC023, BC028, BC029, and BC036.
This device is manufactured by Shenzhen Kingboom Technology Co., Ltd. and has received FDA 510(k) clearance with the number K260147. It is classified as a Pump, Portable, Aspiration (Manual Or Powered) device and is intended for use in General and Plastic Surgery specialties. The device is regulated under product code BTA and regulation number 878.4780.
Other devices from Shenzhen Kingboom Technology Co., Ltd.
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Questions
AI-generated answers, 22 Sep 2026
What is the Electric Nasal Aspirator used for?
The Electric Nasal Aspirator is a portable pump device designed for medical aspiration of nasal secretions. It is intended for use in medical settings to remove nasal secretions in General and Plastic Surgery specialties.
What models of the Electric Nasal Aspirator are available?
The device is available in multiple model numbers including BC026, BC025, BC023, BC028, BC029, and BC036. Each model serves the same primary function of nasal aspiration but may have specific design variations.
What is the regulatory status of this device?
The Electric Nasal Aspirator has received FDA 510(k) clearance with the number K260147. It is classified as a Pump, Portable, Aspiration (Manual Or Powered) device and is regulated under product code BTA and regulation number 878.4780.
Who manufactures the Electric Nasal Aspirator?
The device is manufactured by Shenzhen Kingboom Technology Co., Ltd., located in Shenzhen, China. The company is responsible for the production and distribution of this medical device.