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FDA 510(k)

Mould Probe MR Safe

K-Number: K241764 · 2025-01-10

ApplicantVarian Medical Systems, Inc.
Decision Date2025-01-10
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Mould Probe MR Safe 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 2025-01-10 under 510(k) number K241764. 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 Mould Probe MR Safe?

Mould Probe MR Safe is a medical device that received FDA 510(k) clearance on 2025-01-10. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K241764.

When did Mould Probe MR Safe receive FDA 510(k) clearance?

Mould Probe MR Safe received FDA 510(k) clearance on 2025-01-10, under 510(k) number K241764.

Who is the listed applicant for Mould Probe MR Safe?

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 Mould Probe MR Safe?

The FDA product code for Mould Probe MR Safe is JAQ.

Other records listing Varian Medical Systems, Inc. as applicant

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Related Devices (Code: 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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