Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

FDA 510(k)

Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes

N.º K: K221782 · 2023-03-17

SolicitanteMerit Medical Pte. , Ltd.
Fecha de decisión2023-03-17
Código de productoDRS
Comité asesorCV
DecisiónSubstantially Equivalent

Resumen del dispositivo

Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Pte. , Ltd.. It received FDA 510(k) clearance on 2023-03-17 under 510(k) number K221782. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes?

Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes is a medical device that received FDA 510(k) clearance on 2023-03-17. The listed applicant is Merit Medical Pte. , Ltd.. The 510(k) number is K221782.

When did Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes receive FDA 510(k) clearance?

Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes received FDA 510(k) clearance on 2023-03-17, under 510(k) number K221782.

Who is the listed applicant for Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes?

The FDA 510(k) record lists Merit Medical Pte. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes?

The FDA product code for Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes is DRS.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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: DRS)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

K254074TruPressProcerus EnterprisesK242909FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensorsEdwards Lifesciences, LLCK172458HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer KitSmiths Medical Asd, Inc.K163172HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer KitSmiths Medical Asd, Inc.K161408Compass Cast and MAPCenturion Medical Products CorporationK152472Disposable Pressure TransducerZhejiang Haisheng Medical Device Co., Ltd.

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

↑