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FDA 510(k)

NEXCOMP AND META ETCHANT

K-Number: K080305 · 2008-04-07

ApplicantMeta Biomed Co., Ltd.
Decision Date2008-04-07
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NEXCOMP AND META ETCHANT is the device name listed in this FDA 510(k) record. The listed applicant is Meta Biomed Co., Ltd.. It received FDA 510(k) clearance on 2008-04-07 under 510(k) number K080305. 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 NEXCOMP AND META ETCHANT?

NEXCOMP AND META ETCHANT is a medical device that received FDA 510(k) clearance on 2008-04-07. The listed applicant is Meta Biomed Co., Ltd.. The 510(k) number is K080305.

When did NEXCOMP AND META ETCHANT receive FDA 510(k) clearance?

NEXCOMP AND META ETCHANT received FDA 510(k) clearance on 2008-04-07, under 510(k) number K080305.

Who is the listed applicant for NEXCOMP AND META ETCHANT?

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

What is the FDA product code for NEXCOMP AND META ETCHANT?

The FDA product code for NEXCOMP AND META ETCHANT 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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