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FDA 510(k)

ART-Plan

K-Number: K230023 · 2023-04-19

ApplicantTherapanacea Sas
Decision Date2023-04-19
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ART-Plan is the device name listed in this FDA 510(k) record. The listed applicant is Therapanacea Sas. It received FDA 510(k) clearance on 2023-04-19 under 510(k) number K230023. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ART-Plan?

ART-Plan is a medical device that received FDA 510(k) clearance on 2023-04-19. The listed applicant is Therapanacea Sas. The 510(k) number is K230023.

When did ART-Plan receive FDA 510(k) clearance?

ART-Plan received FDA 510(k) clearance on 2023-04-19, under 510(k) number K230023.

Who is the listed applicant for ART-Plan?

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

What is the FDA product code for ART-Plan?

The FDA product code for ART-Plan is QKB.

Other records listing Therapanacea Sas 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.

K253091ART-Plan+ (v3.1.0)K242822ART-Plan+ (v.3.0.0)K234068ART-Plan (v.2.2.0)

Related Devices (Code: QKB)

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.

K262452AutoContour (RADAC V6)Radformation, Inc.K261306AI Contouring (VA10A)Varian Medical SystemsK260528OncoStudioOncosoft. Inc.,K252548AI-Rad Companion Organs RTSiemens Healthcare GmbHK252190DeepBT Detector-PlusAitewan Biomedical Technology, Inc.K253270Contour ProtégéAI+Mim Software, 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.

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