1717SCV, 1717SGV
K-Number: K201796 · 2020-07-23
ApplicantRayence Co., Ltd.
Decision Date2020-07-23
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
1717SCV, 1717SGV is a medical device manufactured by Rayence Co., Ltd.. It received FDA 510(k) clearance on 2020-07-23 under approval number K201796. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the 1717SCV, 1717SGV?
1717SCV, 1717SGV is a medical device that received FDA 510(k) clearance on 2020-07-23. It is manufactured by Rayence Co., Ltd.. The 510(k) number is K201796.
When was 1717SCV, 1717SGV approved by the FDA?
1717SCV, 1717SGV received FDA 510(k) clearance on 2020-07-23, under approval number K201796.
What company makes 1717SCV, 1717SGV?
1717SCV, 1717SGV is manufactured by Rayence Co., Ltd..
What is the FDA product code for 1717SCV, 1717SGV?
The FDA product code for 1717SCV, 1717SGV is MQB.
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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.