Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

FDA 510(k)

Silla de Ruedas Eléctrica, Joy Rider

N.º K: K220156 · 2022-10-07

SolicitanteTung Keng Enterprise Co., Ltd.
Fecha de decisión2022-10-07
Código de productoITI
Comité asesorPM
DecisiónSubstantially Equivalent

Resumen del dispositivo

Electrically Powered Wheelchair, Joy Rider is the device name listed in this FDA 510(k) record. The listed applicant is Tung Keng Enterprise Co., Ltd.. It received FDA 510(k) clearance on 2022-10-07 under 510(k) number K220156. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Electrically Powered Wheelchair, Joy Rider?

Electrically Powered Wheelchair, Joy Rider is a medical device that received FDA 510(k) clearance on 2022-10-07. The listed applicant is Tung Keng Enterprise Co., Ltd.. The 510(k) number is K220156.

When did Electrically Powered Wheelchair, Joy Rider receive FDA 510(k) clearance?

Electrically Powered Wheelchair, Joy Rider received FDA 510(k) clearance on 2022-10-07, under 510(k) number K220156.

Who is the listed applicant for Electrically Powered Wheelchair, Joy Rider?

The FDA 510(k) record lists Tung Keng Enterprise Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Electrically Powered Wheelchair, Joy Rider?

The FDA product code for Electrically Powered Wheelchair, Joy Rider is ITI.

Ensayos clínicos relacionados

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Dispositivos relacionados (Código: ITI)

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.

K262582Electric wheelchair (GP100)Suzhou Green Pine Medical Co., Ltd.K262054Electric WheelchairYongkang Joymax Medical Technology Co., Ltd.K260053Power Wheelchair (OS-R-M01I)Beijing OrionStar Technology Co., Ltd.K260229Electric wheelchair (HC819N, HC830N, HC831N)Yongkang Hengyi Vehicle Co., Ltd.K261354Electric wheelchair (D03)Foshan Sowell Medical Technology Co., Ltd.K261149Electric Wheelchair (DY611A-2, DY612A-1)Zhejiang Lumbre Electric Appliance Co., Ltd.

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.

↑