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FDA 510(k)

Electric nasal aspirator

K-Number: K222547 · 2022-10-20

Decision Date2022-10-20
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Electric nasal aspirator is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Xinlianfeng Technology Co.,Ltd. It received FDA 510(k) clearance on 2022-10-20 under 510(k) number K222547. 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?

Electric nasal aspirator is a medical device that received FDA 510(k) clearance on 2022-10-20. The listed applicant is Shenzhen Xinlianfeng Technology Co.,Ltd. The 510(k) number is K222547.

When did Electric nasal aspirator receive FDA 510(k) clearance?

Electric nasal aspirator received FDA 510(k) clearance on 2022-10-20, under 510(k) number K222547.

Who is the listed applicant for Electric nasal aspirator?

The FDA 510(k) record lists Shenzhen Xinlianfeng 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?

The FDA product code for Electric nasal aspirator 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.