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FDA 510(k)

Radiation Planning Assistant (RPA)

K-Number: K222728 · 2023-05-17

ApplicantUniversity of Texas, MD Anderson Cancer Center
Decision Date2023-05-17
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Radiation Planning Assistant (RPA) is the device name listed in this FDA 510(k) record. The listed applicant is University of Texas, MD Anderson Cancer Center. It received FDA 510(k) clearance on 2023-05-17 under 510(k) number K222728. 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 Radiation Planning Assistant (RPA)?

Radiation Planning Assistant (RPA) is a medical device that received FDA 510(k) clearance on 2023-05-17. The listed applicant is University of Texas, MD Anderson Cancer Center. The 510(k) number is K222728.

When did Radiation Planning Assistant (RPA) receive FDA 510(k) clearance?

Radiation Planning Assistant (RPA) received FDA 510(k) clearance on 2023-05-17, under 510(k) number K222728.

Who is the listed applicant for Radiation Planning Assistant (RPA)?

The FDA 510(k) record lists University of Texas, MD Anderson Cancer Center as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Radiation Planning Assistant (RPA)?

The FDA product code for Radiation Planning Assistant (RPA) is MUJ.

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.

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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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