PMA de la FDA

lente intraocular

Número de PMA: P990013 · 2021-07-19

SolicitanteStarr Surgical Co.

Fecha de decisión2021-07-19

Número PMAP990013

Código de productoHQL

Clase del dispositivoClase 3

Especialidad médicaO

Número de regulación21 CFR 8

Comité asesorOP

Resumen del dispositivo

intraocular lens is the device name listed in this FDA 510(k) record. The listed applicant is Starr Surgical Co.. It received FDA 510(k) clearance on 2021-07-19. The device is classified under product code HQL. It was reviewed by the OP advisory panel.

Preguntas frecuentes

What is the intraocular lens?

intraocular lens is a medical device that received FDA 510(k) clearance on 2021-07-19. The listed applicant is Starr Surgical Co..

When did intraocular lens receive FDA 510(k) clearance?

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

Who is the listed applicant for intraocular lens?

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

What is the FDA product code for intraocular lens?

The FDA product code for intraocular lens is HQL.

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.