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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 a medical device manufactured by Varian Medical Systems. It received FDA 510(k) clearance on 2023-09-08 under approval 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. It is manufactured by Varian Medical Systems. The 510(k) number is K232400.

When was VariSeed (v10) approved by the FDA?

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

What company makes VariSeed (v10)?

VariSeed (v10) is manufactured by Varian Medical Systems.

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

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

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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.

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