MAZIC Duro
K-Number: K163346 · 2017-03-17
ApplicantVericom Co., Ltd.
Decision Date2017-03-17
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
MAZIC Duro is a medical device manufactured by Vericom Co., Ltd.. It received FDA 510(k) clearance on 2017-03-17 under approval number K163346. 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 MAZIC Duro?
MAZIC Duro is a medical device that received FDA 510(k) clearance on 2017-03-17. It is manufactured by Vericom Co., Ltd.. The 510(k) number is K163346.
When was MAZIC Duro approved by the FDA?
MAZIC Duro received FDA 510(k) clearance on 2017-03-17, under approval number K163346.
What company makes MAZIC Duro?
MAZIC Duro is manufactured by Vericom Co., Ltd..
What is the FDA product code for MAZIC Duro?
The FDA product code for MAZIC Duro 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.