1417WGC_127um and 1417WGC_140um
K-Number: K171417 · 2017-06-12
ApplicantRayence Co., Ltd.
Decision Date2017-06-12
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
1417WGC_127um and 1417WGC_140um is a medical device manufactured by Rayence Co., Ltd.. It received FDA 510(k) clearance on 2017-06-12 under approval number K171417. 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 1417WGC_127um and 1417WGC_140um?
1417WGC_127um and 1417WGC_140um is a medical device that received FDA 510(k) clearance on 2017-06-12. It is manufactured by Rayence Co., Ltd.. The 510(k) number is K171417.
When was 1417WGC_127um and 1417WGC_140um approved by the FDA?
1417WGC_127um and 1417WGC_140um received FDA 510(k) clearance on 2017-06-12, under approval number K171417.
What company makes 1417WGC_127um and 1417WGC_140um?
1417WGC_127um and 1417WGC_140um is manufactured by Rayence Co., Ltd..
What is the FDA product code for 1417WGC_127um and 1417WGC_140um?
The FDA product code for 1417WGC_127um and 1417WGC_140um 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.