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FDA 510(k)

CUI FEATHERED SILICONE MALAR

K-Number: K904348 · 1990-11-26

ApplicantCui Corp.
Decision Date1990-11-26
Product CodeLZK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CUI FEATHERED SILICONE MALAR is the device name listed in this FDA 510(k) record. The listed applicant is Cui Corp.. It received FDA 510(k) clearance on 1990-11-26 under 510(k) number K904348. The device is classified under product code LZK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUI FEATHERED SILICONE MALAR?

CUI FEATHERED SILICONE MALAR 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 K904348.

When did CUI FEATHERED SILICONE MALAR receive FDA 510(k) clearance?

CUI FEATHERED SILICONE MALAR received FDA 510(k) clearance on 1990-11-26, under 510(k) number K904348.

Who is the listed applicant for CUI FEATHERED SILICONE MALAR?

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 FEATHERED SILICONE MALAR?

The FDA product code for CUI FEATHERED SILICONE MALAR is LZK.

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.

View all 7 devices →

Related Devices (Code: LZK)

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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