Data da decisão2018-11-07
Código do produtoDSA
Comité consultivoCV
DecisãoSubstantially Equivalent
Resumo do dispositivo
Curbell branded Patient Monitoring Cables is the device name listed in this FDA 510(k) record. The listed applicant is Curbell Medical Products, Inc.. It received FDA 510(k) clearance on 2018-11-07 under 510(k) number K182220. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Perguntas frequentes
What is the Curbell branded Patient Monitoring Cables?
Curbell branded Patient Monitoring Cables is a medical device that received FDA 510(k) clearance on 2018-11-07. The listed applicant is Curbell Medical Products, Inc.. The 510(k) number is K182220.
When did Curbell branded Patient Monitoring Cables receive FDA 510(k) clearance?
Curbell branded Patient Monitoring Cables received FDA 510(k) clearance on 2018-11-07, under 510(k) number K182220.
Who is the listed applicant for Curbell branded Patient Monitoring Cables?
The FDA 510(k) record lists Curbell Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Curbell branded Patient Monitoring Cables?
The FDA product code for Curbell branded Patient Monitoring Cables is DSA.
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.
Dispositivos Relacionados (Código: DSA)
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.
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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.