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FDA 510(k)

CLEARFIL PHOTO CORE PLT

K-Number: K033970 · 2004-03-26

ApplicantKuraray Medical, Inc.
Decision Date2004-03-26
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CLEARFIL PHOTO CORE PLT 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 2004-03-26 under 510(k) number K033970. 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 PLT?

CLEARFIL PHOTO CORE PLT is a medical device that received FDA 510(k) clearance on 2004-03-26. The listed applicant is Kuraray Medical, Inc.. The 510(k) number is K033970.

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

CLEARFIL PHOTO CORE PLT received FDA 510(k) clearance on 2004-03-26, under 510(k) number K033970.

Who is the listed applicant for CLEARFIL PHOTO CORE PLT?

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 PHOTO CORE PLT?

The FDA product code for CLEARFIL PHOTO CORE PLT is EBF.

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Related Devices (Code: 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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