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FDA 510(k)

Electric Nasal Aspirator (DT10 and DT50, DX80, DX85, DX86 and DX90)

K-Number: K253107 · 2026-04-14

Decision Date2026-04-14
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Electric Nasal Aspirator (DT10 and DT50, DX80, DX85, DX86 and DX90) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Dongjiang Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-04-14 under 510(k) number K253107. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Electric Nasal Aspirator (DT10 and DT50, DX80, DX85, DX86 and DX90)?

Electric Nasal Aspirator (DT10 and DT50, DX80, DX85, DX86 and DX90) is a medical device that received FDA 510(k) clearance on 2026-04-14. The listed applicant is Shenzhen Dongjiang Technology Co., Ltd.. The 510(k) number is K253107.

When did Electric Nasal Aspirator (DT10 and DT50, DX80, DX85, DX86 and DX90) receive FDA 510(k) clearance?

Electric Nasal Aspirator (DT10 and DT50, DX80, DX85, DX86 and DX90) received FDA 510(k) clearance on 2026-04-14, under 510(k) number K253107.

Who is the listed applicant for Electric Nasal Aspirator (DT10 and DT50, DX80, DX85, DX86 and DX90)?

The FDA 510(k) record lists Shenzhen Dongjiang Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Electric Nasal Aspirator (DT10 and DT50, DX80, DX85, DX86 and DX90)?

The FDA product code for Electric Nasal Aspirator (DT10 and DT50, DX80, DX85, DX86 and DX90) is BTA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: BTA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.