LEXATITE QUICK ACRYLIC
K-Number: K033432 · 2004-01-15
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Device Summary
Frequently Asked Questions
What is the LEXATITE QUICK ACRYLIC?
LEXATITE QUICK ACRYLIC is a medical device that received FDA 510(k) clearance on 2004-01-15. The listed applicant is Imtec Corp.. The 510(k) number is K033432.
When did LEXATITE QUICK ACRYLIC receive FDA 510(k) clearance?
LEXATITE QUICK ACRYLIC received FDA 510(k) clearance on 2004-01-15, under 510(k) number K033432.
Who is the listed applicant for LEXATITE QUICK ACRYLIC?
The FDA 510(k) record lists Imtec Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LEXATITE QUICK ACRYLIC?
The FDA product code for LEXATITE QUICK ACRYLIC is EBG.
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 Imtec 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: EBG)
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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