Geon (S2) Nasal Aspirator
K-Number: K243138 · 2025-02-04
Device Summary
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. The listed applicant is Geon Corporation. The 510(k) number is K243138.
When did Geon (S2) Nasal Aspirator receive FDA 510(k) clearance?
Geon (S2) Nasal Aspirator received FDA 510(k) clearance on 2025-02-04, under 510(k) number K243138.
Who is the listed applicant for Geon (S2) Nasal Aspirator?
The FDA 510(k) record lists Geon Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Geon (S2) Nasal Aspirator?
The FDA product code for Geon (S2) Nasal Aspirator is BTA.
Other records listing Geon Corporation as applicant
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.