Data da decisão2022-03-26
Código do produtoLZA
Comité consultivoHO
DecisãoSubstantially Equivalent
Resumo do dispositivo
Clover Glove is the device name listed in this FDA 510(k) record. The listed applicant is Clover Glove Company Limited. It received FDA 510(k) clearance on 2022-03-26 under 510(k) number K213729. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Perguntas frequentes
What is the Clover Glove?
Clover Glove is a medical device that received FDA 510(k) clearance on 2022-03-26. The listed applicant is Clover Glove Company Limited. The 510(k) number is K213729.
When did Clover Glove receive FDA 510(k) clearance?
Clover Glove received FDA 510(k) clearance on 2022-03-26, under 510(k) number K213729.
Who is the listed applicant for Clover Glove?
The FDA 510(k) record lists Clover Glove Company Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Clover Glove?
The FDA product code for Clover Glove is LZA.
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: LZA)
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.