CUI CURVILINEAR SILICONE CHIN
K-Number: K904349 · 1990-11-26
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Device Summary
Frequently Asked Questions
What is the CUI CURVILINEAR SILICONE CHIN?
CUI CURVILINEAR SILICONE CHIN is a medical device that received FDA 510(k) clearance on 1990-11-26. The listed applicant is Cui Corp.. The 510(k) number is K904349.
When did CUI CURVILINEAR SILICONE CHIN receive FDA 510(k) clearance?
CUI CURVILINEAR SILICONE CHIN received FDA 510(k) clearance on 1990-11-26, under 510(k) number K904349.
Who is the listed applicant for CUI CURVILINEAR SILICONE CHIN?
The FDA 510(k) record lists Cui Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CUI CURVILINEAR SILICONE CHIN?
The FDA product code for CUI CURVILINEAR SILICONE CHIN is FWP.
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 Cui Corp. 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: FWP)
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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