star RF Electrode, VIVA RF Electrode
K-Number: K172012 · 2018-03-14
ApplicantStarmed Co., Ltd.
Decision Date2018-03-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
star RF Electrode, VIVA RF Electrode is a medical device manufactured by Starmed Co., Ltd.. It received FDA 510(k) clearance on 2018-03-14 under approval number K172012. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the star RF Electrode, VIVA RF Electrode?
star RF Electrode, VIVA RF Electrode is a medical device that received FDA 510(k) clearance on 2018-03-14. It is manufactured by Starmed Co., Ltd.. The 510(k) number is K172012.
When was star RF Electrode, VIVA RF Electrode approved by the FDA?
star RF Electrode, VIVA RF Electrode received FDA 510(k) clearance on 2018-03-14, under approval number K172012.
What company makes star RF Electrode, VIVA RF Electrode?
star RF Electrode, VIVA RF Electrode is manufactured by Starmed Co., Ltd..
What is the FDA product code for star RF Electrode, VIVA RF Electrode?
The FDA product code for star RF Electrode, VIVA RF Electrode is GEI.
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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.