FDA 510(k)

ART-PLAN

N.º K: K220813 · 2022-06-17

Fecha de decisión2022-06-17

Código de productoQKB

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

ART-PLAN is the device name listed in this FDA 510(k) record. The listed applicant is Therapanacea. It received FDA 510(k) clearance on 2022-06-17 under 510(k) number K220813. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ART-PLAN?

ART-PLAN is a medical device that received FDA 510(k) clearance on 2022-06-17. The listed applicant is Therapanacea. The 510(k) number is K220813.

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

ART-PLAN received FDA 510(k) clearance on 2022-06-17, under 510(k) number K220813.

Who is the listed applicant for ART-PLAN?

The FDA 510(k) record lists Therapanacea 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.

Otros registros que enlistan a Therapanacea como solicitante

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

K232479ART-Plan K202700ART-Plan

Dispositivos relacionados (Código: QKB)

K262452AutoContour (RADAC V6)Radformation, Inc.K261306AI Contouring (VA10A)Varian Medical Systems K260528OncoStudioOncosoft. Inc.,K252548AI-Rad Companion Órganos RTSiemens Healthcare GmbH K252190DeepBT Detector-PlusAitewan Biomedical Technology, Inc.K253270Contour ProtégéAI+Mim Software, Inc.

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.