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FDA 510(k)

Nasal Aspirator (TLC-N02); Electric NoseFrida Pro (12300400); Electric NoseFrida (12100401)

K-Number: K262822 · 2026-10-07

Decision Date2026-10-07
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Nasal Aspirator (TLC-N02); Electric NoseFrida Pro (12300400); Electric NoseFrida (12100401) is the device name listed in this FDA 510(k) record. The listed applicant is Zhongshan GL Electronics Co. , Ltd.. It received FDA 510(k) clearance on 2026-10-07 under 510(k) number K262822. 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 Nasal Aspirator (TLC-N02); Electric NoseFrida Pro (12300400); Electric NoseFrida (12100401)?

Nasal Aspirator (TLC-N02); Electric NoseFrida Pro (12300400); Electric NoseFrida (12100401) is a medical device that received FDA 510(k) clearance on 2026-10-07. The listed applicant is Zhongshan GL Electronics Co. , Ltd.. The 510(k) number is K262822.

When did Nasal Aspirator (TLC-N02); Electric NoseFrida Pro (12300400); Electric NoseFrida (12100401) receive FDA 510(k) clearance?

Nasal Aspirator (TLC-N02); Electric NoseFrida Pro (12300400); Electric NoseFrida (12100401) received FDA 510(k) clearance on 2026-10-07, under 510(k) number K262822.

Who is the listed applicant for Nasal Aspirator (TLC-N02); Electric NoseFrida Pro (12300400); Electric NoseFrida (12100401)?

The FDA 510(k) record lists Zhongshan GL Electronics Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nasal Aspirator (TLC-N02); Electric NoseFrida Pro (12300400); Electric NoseFrida (12100401)?

The FDA product code for Nasal Aspirator (TLC-N02); Electric NoseFrida Pro (12300400); Electric NoseFrida (12100401) 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.

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