RCT800
K-Number: K182805 · 2018-12-14
ApplicantRay Co., Ltd.
Decision Date2018-12-14
Product CodeOAS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
RCT800 is a medical device manufactured by Ray Co., Ltd.. It received FDA 510(k) clearance on 2018-12-14 under approval number K182805. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the RCT800?
RCT800 is a medical device that received FDA 510(k) clearance on 2018-12-14. It is manufactured by Ray Co., Ltd.. The 510(k) number is K182805.
When was RCT800 approved by the FDA?
RCT800 received FDA 510(k) clearance on 2018-12-14, under approval number K182805.
What company makes RCT800?
RCT800 is manufactured by Ray Co., Ltd..
What is the FDA product code for RCT800?
The FDA product code for RCT800 is OAS.
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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.