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FDA 510(k)

VariSeed (v10)

K-Number: K232400 · 2023-09-08

ApplicantVarian Medical Systems
Decision Date2023-09-08
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VariSeed (v10) is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems. It received FDA 510(k) clearance on 2023-09-08 under 510(k) number K232400. 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 VariSeed (v10)?

VariSeed (v10) is a medical device that received FDA 510(k) clearance on 2023-09-08. The listed applicant is Varian Medical Systems. The 510(k) number is K232400.

When did VariSeed (v10) receive FDA 510(k) clearance?

VariSeed (v10) received FDA 510(k) clearance on 2023-09-08, under 510(k) number K232400.

Who is the listed applicant for VariSeed (v10)?

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

What is the FDA product code for VariSeed (v10)?

The FDA product code for VariSeed (v10) is MUJ.

Other records listing Varian Medical Systems as applicant

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Related Devices (Code: MUJ)

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.

K260750Virtual Cone (1.0)Varian Medical Systems, Inc.K253050RadOncAIInformaiK260207Multimodality 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.

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