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 PMA

System, colorectal neoplasia, DNA methylation and hemoglobin detection

Número do PMA: P230009 · 2026-09-16

RequerenteGuardant Health, Inc.
Data da decisão2026-09-16
Número PMAP230009
Código do produtoPHP
Classe do DispositivoClasse 3
Especialidade MédicaU
Comité consultivoMG

Resumo do dispositivo

System, colorectal neoplasia, DNA methylation and hemoglobin detection is the device name listed in this FDA 510(k) record. The listed applicant is Guardant Health, Inc.. It received FDA 510(k) clearance on 2026-09-16. The device is classified under product code PHP. It was reviewed by the MG advisory panel.

Perguntas frequentes

What is the System, colorectal neoplasia, DNA methylation and hemoglobin detection?

System, colorectal neoplasia, DNA methylation and hemoglobin detection is a medical device that received FDA 510(k) clearance on 2026-09-16. The listed applicant is Guardant Health, Inc..

When did System, colorectal neoplasia, DNA methylation and hemoglobin detection receive FDA 510(k) clearance?

The clearance date for System, colorectal neoplasia, DNA methylation and hemoglobin detection can be found in the official FDA records.

Who is the listed applicant for System, colorectal neoplasia, DNA methylation and hemoglobin detection?

The FDA 510(k) record lists Guardant Health, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for System, colorectal neoplasia, DNA methylation and hemoglobin detection?

The FDA product code for System, colorectal neoplasia, DNA methylation and hemoglobin detection is PHP.

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.

↑