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FDA 510(k)

RCT700

K-Number: K182614 · 2018-10-16

ApplicantRay Co., Ltd.
Decision Date2018-10-16
Product CodeOAS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RCT700 is the device name listed in this FDA 510(k) record. The listed applicant is Ray Co., Ltd.. It received FDA 510(k) clearance on 2018-10-16 under 510(k) number K182614. 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 2018-10-16. The listed applicant is Ray Co., Ltd.. The 510(k) number is K182614.

When did RCT700 receive FDA 510(k) clearance?

RCT700 received FDA 510(k) clearance on 2018-10-16, under 510(k) number K182614.

Who is the listed applicant for RCT700?

The FDA 510(k) record lists Ray Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RCT700?

The FDA product code for RCT700 is OAS.

Other records listing Ray Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260462RCT800K251798RCT700K251109SMARTDentK243903RCT600K233625RAYDENT SWK232325RAYSCAN a-Expert

View all 17 devices →

Related Devices (Code: OAS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261748Dental Cone-beam Computed Tomography (mDX-15P Series)Hefei Meyer Optoelectronic Technology, Inc.K250839Dental X-ray SystemChangzhou Boen Zhongding Medical Technology Co., Ltd.K260662Dental Cone Beam Computed Tomography SystemYofo Medical Technology Co., Ltd.K253935medXion NEXUSmedXion Technologies, Inc.K260462RCT800Ray Co., Ltd.K260093Green X 12 VE (PHT-70CHS); Green X VE (PHT-70CHS)VATECH Co., Ltd.

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.

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