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FDA 510(k)

EPRICORD

K-Number: K033267 · 2003-12-22

ApplicantKuraray Medical, Inc.
Decision Date2003-12-22
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EPRICORD 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 2003-12-22 under 510(k) number K033267. 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 EPRICORD?

EPRICORD is a medical device that received FDA 510(k) clearance on 2003-12-22. The listed applicant is Kuraray Medical, Inc.. The 510(k) number is K033267.

When did EPRICORD receive FDA 510(k) clearance?

EPRICORD received FDA 510(k) clearance on 2003-12-22, under 510(k) number K033267.

Who is the listed applicant for EPRICORD?

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 EPRICORD?

The FDA product code for EPRICORD 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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