Baby Nasal Aspirator (BN002); Baby Nasal Aspirator (BN006); Baby Nasal Aspirator (BN007); Baby Nasal Aspirator (BN008); Baby Nasal Aspirator (BN009)

FDA 510(k) K251450 · Shenzhen Desida Technology Co., Ltd.

Substantially Equivalent

510(k) numberK251450

Submission

Device name
Baby Nasal Aspirator (BN002); Baby Nasal Aspirator (BN006); Baby Nasal Aspirator (BN007); Baby Nasal Aspirator (BN008); Baby Nasal Aspirator (BN009)
Applicant
Shenzhen Desida Technology Co., Ltd.
Shenzhen, CN
Received
May 9, 2025
Decision date
June 6, 2025
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

Other 510(k)s with product code BTA

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K251101AIRO Suction Unit (AIRO-01)BTA · Traditional Cro, LLC04/26/2025SE
K250697Electric Nasal Aspirator (BC026, BC025, BC023)BTA · Traditional Shenzhen Kingboom Technology Co., Ltd.04/23/2025SE
K241799ATMOS C 051 Thorax (317.0200.0); Secretion canister 800ml (317.1300.0); Hose system…BTA · Traditional Atmos Medizintechnik GmbH & Co. KG03/07/2025SE

More from Atmos Medizintechnik GmbH & Co. KG

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K254079LED Light Therapy Mask (Models: T2, RLD10)OHS · Traditional 03/16/2026SE
K244033Electric Nasal Aspirator (NASA601,NASA602,NASA603,NASA605,NASA606,NASA608,NASA610)BTA · Traditional 05/16/2025SE
K233901Baby Nasal Aspirator (KA1006, KA1001, KA1005, NASA005, NASA006, NASA008, NASA009)BTA · Traditional 03/20/2024SE
K221643Hair Removal Device (Model: IPL-D26, IPL-D19)OHT · Traditional 10/21/2022SE
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Questions and answers

When was Baby Nasal Aspirator (BN002); Baby Nasal Aspirator (BN006); Baby Nasal Aspirator (BN007); Baby Nasal Aspirator (BN008); Baby Nasal Aspirator (BN009) cleared by the FDA?

Baby Nasal Aspirator (BN002); Baby Nasal Aspirator (BN006); Baby Nasal Aspirator (BN007); Baby Nasal Aspirator (BN008); Baby Nasal Aspirator (BN009) (K251450) received a 510(k) decision of Substantially Equivalent on June 6, 2025, 28 days after the submission was received.

What is the product code of K251450?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.