FDA 510(k)

Geon (S2) Nasal Aspirator

K-Number: K243138 · 2025-02-04

Decision Date2025-02-04

Product CodeBTA

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Geon (S2) Nasal Aspirator is a medical device manufactured by Geon Corporation. It received FDA 510(k) clearance on 2025-02-04 under approval number K243138. 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 Geon (S2) Nasal Aspirator?

Geon (S2) Nasal Aspirator is a medical device that received FDA 510(k) clearance on 2025-02-04. It is manufactured by Geon Corporation. The 510(k) number is K243138.

When was Geon (S2) Nasal Aspirator approved by the FDA?

Geon (S2) Nasal Aspirator received FDA 510(k) clearance on 2025-02-04, under approval number K243138.

What company makes Geon (S2) Nasal Aspirator?

Geon (S2) Nasal Aspirator is manufactured by Geon Corporation.

What is the FDA product code for Geon (S2) Nasal Aspirator?

The FDA product code for Geon (S2) Nasal Aspirator is BTA.

Related Clinical Trials

NCT06816875 Comparison of the User Experience of Four Nasal Aspirators in Infants COMPLETED

Other Devices by Geon Corporation

K220126Geonic Nasal Aspirator, Geonic Nasal Cleaner

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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.