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FDA 510(k)

Guided Aarhus Applicator Set

K-Number: K252884 · 2025-11-19

ApplicantVarian Medical Systems
Decision Date2025-11-19
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Guided Aarhus Applicator Set is a medical device manufactured by Varian Medical Systems. It received FDA 510(k) clearance on 2025-11-19 under approval number K252884. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Guided Aarhus Applicator Set?

Guided Aarhus Applicator Set is a medical device that received FDA 510(k) clearance on 2025-11-19. It is manufactured by Varian Medical Systems. The 510(k) number is K252884.

When was Guided Aarhus Applicator Set approved by the FDA?

Guided Aarhus Applicator Set received FDA 510(k) clearance on 2025-11-19, under approval number K252884.

What company makes Guided Aarhus Applicator Set?

Guided Aarhus Applicator Set is manufactured by Varian Medical Systems.

What is the FDA product code for Guided Aarhus Applicator Set?

The FDA product code for Guided Aarhus Applicator Set is JAQ.

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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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