NASALCEASE
K-Number: K041446 · 2004-07-01
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Device Summary
Frequently Asked Questions
What is the NASALCEASE?
NASALCEASE is a medical device that received FDA 510(k) clearance on 2004-07-01. The listed applicant is Les Laboratorires Brothier, S.A.. The 510(k) number is K041446.
When did NASALCEASE receive FDA 510(k) clearance?
NASALCEASE received FDA 510(k) clearance on 2004-07-01, under 510(k) number K041446.
Who is the listed applicant for NASALCEASE?
The FDA 510(k) record lists Les Laboratorires Brothier, S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NASALCEASE?
The FDA product code for NASALCEASE is EMX.
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.
Other records listing Les Laboratorires Brothier, S.A. 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: EMX)
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.
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