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)

AIK Agulhas de Acupunctura Estéreis para Uso Único

Número K: K162566 · 2017-05-11

RequerenteChangchun Aik Medical Devices Co., Ltd.
Data da decisão2017-05-11
Código do produtoMQX
Comité consultivoHO
DecisãoSubstantially Equivalent

Resumo do dispositivo

AIK Sterile Acupuncture Needles for Single Use is the device name listed in this FDA 510(k) record. The listed applicant is Changchun Aik Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2017-05-11 under 510(k) number K162566. The device is classified under product code MQX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the AIK Sterile Acupuncture Needles for Single Use?

AIK Sterile Acupuncture Needles for Single Use is a medical device that received FDA 510(k) clearance on 2017-05-11. The listed applicant is Changchun Aik Medical Devices Co., Ltd.. The 510(k) number is K162566.

When did AIK Sterile Acupuncture Needles for Single Use receive FDA 510(k) clearance?

AIK Sterile Acupuncture Needles for Single Use received FDA 510(k) clearance on 2017-05-11, under 510(k) number K162566.

Who is the listed applicant for AIK Sterile Acupuncture Needles for Single Use?

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

What is the FDA product code for AIK Sterile Acupuncture Needles for Single Use?

The FDA product code for AIK Sterile Acupuncture Needles for Single Use is MQX.

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

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.

↑