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FDA 510(k)

Nexcomp

K-Number: K181689 · 2018-11-15

ApplicantMeta Biomed Co., Ltd.
Decision Date2018-11-15
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Nexcomp 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 2018-11-15 under 510(k) number K181689. 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?

Nexcomp is a medical device that received FDA 510(k) clearance on 2018-11-15. The listed applicant is Meta Biomed Co., Ltd.. The 510(k) number is K181689.

When did Nexcomp receive FDA 510(k) clearance?

Nexcomp received FDA 510(k) clearance on 2018-11-15, under 510(k) number K181689.

Who is the listed applicant for Nexcomp?

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?

The FDA product code for Nexcomp is EBF.

Other records listing Meta Biomed Co., Ltd. as applicant

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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.

K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K261246SRGC-06GC America, Inc.K261093DIAFILDiaDent Group InternationalK261071DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW (0.5g)DiaDent Group InternationalK260805Dual CoreVericom Co., Ltd.

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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