RCT700
K-Number: K160525 · 2016-06-20
ApplicantRay Co., Ltd.
Decision Date2016-06-20
Product CodeOAS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
RCT700 is a medical device manufactured by Ray Co., Ltd.. It received FDA 510(k) clearance on 2016-06-20 under approval number K160525. 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 RCT700?
RCT700 is a medical device that received FDA 510(k) clearance on 2016-06-20. It is manufactured by Ray Co., Ltd.. The 510(k) number is K160525.
When was RCT700 approved by the FDA?
RCT700 received FDA 510(k) clearance on 2016-06-20, under approval number K160525.
What company makes RCT700?
RCT700 is manufactured by Ray Co., Ltd..
What is the FDA product code for RCT700?
The FDA product code for RCT700 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.