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 a medical device manufactured by Meta Biomed Co., Ltd.. It received FDA 510(k) clearance on 2018-11-15 under approval 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. It is manufactured by Meta Biomed Co., Ltd.. The 510(k) number is K181689.
When was Nexcomp approved by the FDA?
Nexcomp received FDA 510(k) clearance on 2018-11-15, under approval number K181689.
What company makes Nexcomp?
Nexcomp is manufactured by Meta Biomed Co., Ltd..
What is the FDA product code for Nexcomp?
The FDA product code for Nexcomp 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.