Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MAASTRO Rectal Applicator Set

K-Number: K252717 · 2026-05-20

ApplicantVarian Medical Systems
Decision Date2026-05-20
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAASTRO Rectal Applicator Set is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems. It received FDA 510(k) clearance on 2026-05-20 under 510(k) number K252717. 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 MAASTRO Rectal Applicator Set?

MAASTRO Rectal Applicator Set is a medical device that received FDA 510(k) clearance on 2026-05-20. The listed applicant is Varian Medical Systems. The 510(k) number is K252717.

When did MAASTRO Rectal Applicator Set receive FDA 510(k) clearance?

MAASTRO Rectal Applicator Set received FDA 510(k) clearance on 2026-05-20, under 510(k) number K252717.

Who is the listed applicant for MAASTRO Rectal Applicator Set?

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

What is the FDA product code for MAASTRO Rectal Applicator Set?

The FDA product code for MAASTRO Rectal Applicator Set is JAQ.

Other records listing Varian Medical Systems as applicant

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.

K261856Halcyon, Ethos Radiotherapy System (5.0)K261306AI Contouring (VA10A)K260750Virtual Cone (1.0)K253026Respiratory Gating for Scanners (2.1)K252815ProBeam 360 Proton Therapy System v3.0K252304syngo.via RT Image Suite VC10

View all 96 devices →

Related Devices (Code: JAQ)

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.

K262383LumenCare AzureNucletron B.V.K251037Rectal ApplicatorNucletron B.V.K252884Guided Aarhus Applicator SetVarian Medical SystemsK250299CT/ MR Tandem and Ovoid SetVarian Medical Systems, Inc.K250289Intracavitary/Interstitial SystemVarian Medical SystemsK243939Titanium Flexible Geometry FSD Applicator Set (GM11013400)Varian Medical Systems, Inc.

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.

↑