ACTIPROTECT UC N95 RESPIRATOR
K-Number: K093189 · 2010-07-02
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Device Summary
Frequently Asked Questions
What is the ACTIPROTECT UC N95 RESPIRATOR?
ACTIPROTECT UC N95 RESPIRATOR is a medical device that received FDA 510(k) clearance on 2010-07-02. The listed applicant is Glaxosmithkline Consumer Healthcare. The 510(k) number is K093189.
When did ACTIPROTECT UC N95 RESPIRATOR receive FDA 510(k) clearance?
ACTIPROTECT UC N95 RESPIRATOR received FDA 510(k) clearance on 2010-07-02, under 510(k) number K093189.
Who is the listed applicant for ACTIPROTECT UC N95 RESPIRATOR?
The FDA 510(k) record lists Glaxosmithkline Consumer Healthcare as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACTIPROTECT UC N95 RESPIRATOR?
The FDA product code for ACTIPROTECT UC N95 RESPIRATOR is ORW.
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 Glaxosmithkline Consumer Healthcare 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.
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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