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FDA 510(k)

CLEARFIL ESTHETIC CEMENT & DC BOND

K-Number: K062410 · 2006-09-26

Decision Date2006-09-26
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CLEARFIL ESTHETIC CEMENT & DC BOND is the device name listed in this FDA 510(k) record. The listed applicant is Kuraray Medical, Inc.. It received FDA 510(k) clearance on 2006-09-26 under 510(k) number K062410. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARFIL ESTHETIC CEMENT & DC BOND?

CLEARFIL ESTHETIC CEMENT & DC BOND is a medical device that received FDA 510(k) clearance on 2006-09-26. The listed applicant is Kuraray Medical, Inc.. The 510(k) number is K062410.

When did CLEARFIL ESTHETIC CEMENT & DC BOND receive FDA 510(k) clearance?

CLEARFIL ESTHETIC CEMENT & DC BOND received FDA 510(k) clearance on 2006-09-26, under 510(k) number K062410.

Who is the listed applicant for CLEARFIL ESTHETIC CEMENT & DC BOND?

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

What is the FDA product code for CLEARFIL ESTHETIC CEMENT & DC BOND?

The FDA product code for CLEARFIL ESTHETIC CEMENT & DC BOND is EMA.

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 Kuraray Medical, Inc. 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 42 devices →

Related Devices (Code: EMA)

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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