PMA de la FDA

Fluid, intraocular

Número de PMA: P950008 · 2024-06-03

SolicitanteAlcon

Fecha de decisión2024-06-03

Número PMAP950008

Código de productoLWL

Clase del dispositivoClase 3

Especialidad médicaO

Número de regulación21 CFR 8

Comité asesorOP

Resumen del dispositivo

Fluid, intraocular is the device name listed in this FDA 510(k) record. The listed applicant is Alcon. It received FDA 510(k) clearance on 2024-06-03. The device is classified under product code LWL. It was reviewed by the OP advisory panel.

Preguntas frecuentes

What is the Fluid, intraocular?

Fluid, intraocular is a medical device that received FDA 510(k) clearance on 2024-06-03. The listed applicant is Alcon.

When did Fluid, intraocular receive FDA 510(k) clearance?

The clearance date for Fluid, intraocular can be found in the official FDA records.

Who is the listed applicant for Fluid, intraocular?

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

What is the FDA product code for Fluid, intraocular?

The FDA product code for Fluid, intraocular is LWL.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.