ADSEAL Plus
K-Number: K230010 · 2023-04-13
ApplicantMeta Biomed Co., Ltd.
Decision Date2023-04-13
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
ADSEAL Plus is a medical device manufactured by Meta Biomed Co., Ltd.. It received FDA 510(k) clearance on 2023-04-13 under approval number K230010. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ADSEAL Plus?
ADSEAL Plus is a medical device that received FDA 510(k) clearance on 2023-04-13. It is manufactured by Meta Biomed Co., Ltd.. The 510(k) number is K230010.
When was ADSEAL Plus approved by the FDA?
ADSEAL Plus received FDA 510(k) clearance on 2023-04-13, under approval number K230010.
What company makes ADSEAL Plus?
ADSEAL Plus is manufactured by Meta Biomed Co., Ltd..
What is the FDA product code for ADSEAL Plus?
The FDA product code for ADSEAL Plus is KIF.
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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.