Ezfil
K-Number: K191991 · 2020-03-05
ApplicantMeta Biomed Co., Ltd.
Decision Date2020-03-05
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Ezfil is a medical device manufactured by Meta Biomed Co., Ltd.. It received FDA 510(k) clearance on 2020-03-05 under approval number K191991. 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 Ezfil?
Ezfil is a medical device that received FDA 510(k) clearance on 2020-03-05. It is manufactured by Meta Biomed Co., Ltd.. The 510(k) number is K191991.
When was Ezfil approved by the FDA?
Ezfil received FDA 510(k) clearance on 2020-03-05, under approval number K191991.
What company makes Ezfil?
Ezfil is manufactured by Meta Biomed Co., Ltd..
What is the FDA product code for Ezfil?
The FDA product code for Ezfil 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.