Aviso: Este site agrega dados públicos oficiais da FDA, ClinicalTrials.gov, PubMed e SEC EDGAR apenas para referência geral. Não constitui aconselhamento médico, diagnóstico, recomendação de tratamento ou aconselhamento de investimento.

FDA 510(k)

Cadeira de Rodas de Alumínio Rebatível SYIV 100-LQXAL2482-407

Número K: K213790 · 2022-03-14

RequerenteMobility Source Medical Technology Co., Ltd.
Data da decisão2022-03-14
Código do produtoIOR
Comité consultivoPM
DecisãoSubstantially Equivalent

Resumo do dispositivo

Aluminum back folding wheelchair SYIV 100-LQXAL2482-407 is the device name listed in this FDA 510(k) record. The listed applicant is Mobility Source Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-03-14 under 510(k) number K213790. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Aluminum back folding wheelchair SYIV 100-LQXAL2482-407?

Aluminum back folding wheelchair SYIV 100-LQXAL2482-407 is a medical device that received FDA 510(k) clearance on 2022-03-14. The listed applicant is Mobility Source Medical Technology Co., Ltd.. The 510(k) number is K213790.

When did Aluminum back folding wheelchair SYIV 100-LQXAL2482-407 receive FDA 510(k) clearance?

Aluminum back folding wheelchair SYIV 100-LQXAL2482-407 received FDA 510(k) clearance on 2022-03-14, under 510(k) number K213790.

Who is the listed applicant for Aluminum back folding wheelchair SYIV 100-LQXAL2482-407?

The FDA 510(k) record lists Mobility Source Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Aluminum back folding wheelchair SYIV 100-LQXAL2482-407?

The FDA product code for Aluminum back folding wheelchair SYIV 100-LQXAL2482-407 is IOR.

Ensaios clínicos relacionados

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

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: IOR)

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

K253762ErgoSteel (ES0001/696)Strongback Mobility AG C/O Blueaudit GmbHK261919Multifunctional wheelchair (YJ-059)Zhenjiang Assure Medical Equipment Co., Ltd.K260144Reclining wheelchair (YJ-013L)Zhenjiang Assure Medical Equipment Co., Ltd.K260141Bariatric Heavy Duty Wheelchair (YJ-010V, YJ-010C)Zhenjiang Assure Medical Equipment Co., Ltd.K260145YJ-K1K2 Wheelchair (YJ-013F)Zhenjiang Assure Medical Equipment Co., Ltd.K261571Manual Wheelchair (H008, PCK7)Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.

Fonte oficial

Ver na base de dados da FDA →

Dados provenientes da FDA Open API. Para informações mais recentes e oficiais, consulte sempre o registro oficial.

↑