Well-Root ST
K-Number: K170950 · 2017-12-20
ApplicantVericom Co., Ltd.
Decision Date2017-12-20
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Well-Root ST is a medical device manufactured by Vericom Co., Ltd.. It received FDA 510(k) clearance on 2017-12-20 under approval number K170950. 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 Well-Root ST?
Well-Root ST is a medical device that received FDA 510(k) clearance on 2017-12-20. It is manufactured by Vericom Co., Ltd.. The 510(k) number is K170950.
When was Well-Root ST approved by the FDA?
Well-Root ST received FDA 510(k) clearance on 2017-12-20, under approval number K170950.
What company makes Well-Root ST?
Well-Root ST is manufactured by Vericom Co., Ltd..
What is the FDA product code for Well-Root ST?
The FDA product code for Well-Root ST 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.