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FDA 510(k)

COSMEDENT CORE PASTE

K-Number: K040994 · 2004-06-03

ApplicantCosmedent, Inc.
Decision Date2004-06-03
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COSMEDENT CORE PASTE is the device name listed in this FDA 510(k) record. The listed applicant is Cosmedent, Inc.. It received FDA 510(k) clearance on 2004-06-03 under 510(k) number K040994. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COSMEDENT CORE PASTE?

COSMEDENT CORE PASTE is a medical device that received FDA 510(k) clearance on 2004-06-03. The listed applicant is Cosmedent, Inc.. The 510(k) number is K040994.

When did COSMEDENT CORE PASTE receive FDA 510(k) clearance?

COSMEDENT CORE PASTE received FDA 510(k) clearance on 2004-06-03, under 510(k) number K040994.

Who is the listed applicant for COSMEDENT CORE PASTE?

The FDA 510(k) record lists Cosmedent, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COSMEDENT CORE PASTE?

The FDA product code for COSMEDENT CORE PASTE is EBF.

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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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