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)

Aquilion ServeSP (TSX-307B) V2.0

K-Number: K260078 · 2026-03-13

ApplicantCanon Medical Systems Corporation
Decision Date2026-03-13
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Aquilion ServeSP (TSX-307B) V2.0 is the device name listed in this FDA 510(k) record. The listed applicant is Canon Medical Systems Corporation. It received FDA 510(k) clearance on 2026-03-13 under 510(k) number K260078. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Aquilion ServeSP (TSX-307B) V2.0?

Aquilion ServeSP (TSX-307B) V2.0 is a medical device that received FDA 510(k) clearance on 2026-03-13. The listed applicant is Canon Medical Systems Corporation. The 510(k) number is K260078.

When did Aquilion ServeSP (TSX-307B) V2.0 receive FDA 510(k) clearance?

Aquilion ServeSP (TSX-307B) V2.0 received FDA 510(k) clearance on 2026-03-13, under 510(k) number K260078.

Who is the listed applicant for Aquilion ServeSP (TSX-307B) V2.0?

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

What is the FDA product code for Aquilion ServeSP (TSX-307B) V2.0?

The FDA product code for Aquilion ServeSP (TSX-307B) V2.0 is JAK.

Other records listing Canon Medical Systems Corporation 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.

K253596Aquilion ONE (TSX-308A/TSX-306A) V2.0K253625Vantage Fortian/Orian 1.5T, MRT-1550, V10.0 with AiCE Reconstruction Processing Unit for MRK253584Alphenix, INFX-8000V/B, INFX-8000V/S, V9.6 with aEvolve Imaging (FOV Extension)K253597Aplio beyond and Aplio me Software V2.0 Diagnostic Ultrasound SystemK251370Cartesion Prime (PCD-1000A/3) V10.21K252074Aplio i900, Aplio i800 and Aplio i700 Software V9.0 Diagnostic Ultrasound System

View all 97 devices →

Related Devices (Code: JAK)

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.

K253450BodyTom Elite (NL4000)NeuroLogica Corp., a Samsung CompanyK253770CardIQ SuiteGE Medical Systems SCSK253560Enhanced Boundary for PCCTGe Medical Systems, LLCK253026Respiratory Gating for Scanners (2.1)Varian Medical Systems, Inc.K253596Aquilion ONE (TSX-308A/TSX-306A) V2.0Canon Medical Systems CorporationK253649Spectral CT Verida FamilyPhilips Medical Systems Technologies , Ltd.

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.

↑