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FDA 510(k)

CLEARFIL PHOTO CORE

K-Number: K882006 · 1988-06-13

ApplicantKuraray Co.
Decision Date1988-06-13
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CLEARFIL PHOTO CORE is the device name listed in this FDA 510(k) record. The listed applicant is Kuraray Co.. It received FDA 510(k) clearance on 1988-06-13 under 510(k) number K882006. 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 CLEARFIL PHOTO CORE?

CLEARFIL PHOTO CORE is a medical device that received FDA 510(k) clearance on 1988-06-13. The listed applicant is Kuraray Co.. The 510(k) number is K882006.

When did CLEARFIL PHOTO CORE receive FDA 510(k) clearance?

CLEARFIL PHOTO CORE received FDA 510(k) clearance on 1988-06-13, under 510(k) number K882006.

Who is the listed applicant for CLEARFIL PHOTO CORE?

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

What is the FDA product code for CLEARFIL PHOTO CORE?

The FDA product code for CLEARFIL PHOTO CORE is EBF.

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.

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Other records listing Kuraray Co. 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.

K990040CLEARFIL SE BONDK951813CARIES DETECTORK933030PANAVIA 21K925383PHOTO CLEARFIL OPAQUERK925404CLEARFIL PORCELAIN BOND ACTIVATORK912707CLEARFIL LINER BOND SYSTEM

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Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, Inc.

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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