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FDA 510(k)

CT/ MR Tandem and Ovoid Set

K-Number: K250299 · 2025-05-09

ApplicantVarian Medical Systems, Inc.
Decision Date2025-05-09
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CT/ MR Tandem and Ovoid Set is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2025-05-09 under 510(k) number K250299. 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 CT/ MR Tandem and Ovoid Set?

CT/ MR Tandem and Ovoid Set is a medical device that received FDA 510(k) clearance on 2025-05-09. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K250299.

When did CT/ MR Tandem and Ovoid Set receive FDA 510(k) clearance?

CT/ MR Tandem and Ovoid Set received FDA 510(k) clearance on 2025-05-09, under 510(k) number K250299.

Who is the listed applicant for CT/ MR Tandem and Ovoid Set?

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

What is the FDA product code for CT/ MR Tandem and Ovoid Set?

The FDA product code for CT/ MR Tandem and Ovoid 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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