FDA 510(k)

ONQ RTS

K-Number: K123357 · 2012-12-28

Decision Date2012-12-28

Product CodeMUJ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

ONQ RTS is the device name listed in this FDA 510(k) record. The listed applicant is Oncology Systems, Inc.. It received FDA 510(k) clearance on 2012-12-28 under 510(k) number K123357. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ONQ RTS?

ONQ RTS is a medical device that received FDA 510(k) clearance on 2012-12-28. The listed applicant is Oncology Systems, Inc.. The 510(k) number is K123357.

When did ONQ RTS receive FDA 510(k) clearance?

ONQ RTS received FDA 510(k) clearance on 2012-12-28, under 510(k) number K123357.

Who is the listed applicant for ONQ RTS?

The FDA 510(k) record lists Oncology Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ONQ RTS?

The FDA product code for ONQ RTS is MUJ.

Other records listing Oncology Systems, Inc. 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.

K092522ACU007S K051753ACCU-SOURCE K871810PLAN-32 SOFTWARE

Related Devices (Code: MUJ)

K260750Virtual Cone (1.0)Varian Medical Systems, Inc.K253050RadOncAIInformai K260207Multimodality Simulation Workspace (MM Sim) (v1.0.0)Philips Medical Systems Nederland B.V.K252784eXaSkin PlusAnatomical Geometry S.L.K253078ART.1-USSeetreat Pty, Ltd.K252304syngo.via RT Image Suite VC10Varian Medical Systems, Inc.

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.