FDA PMA

lente intraocular

Número do PMA: P190018 · 2026-08-17

RequerenteAlcon Laboratories, LLC

Data da decisão2026-08-17

Número PMAP190018

Código do produtoHQL

Classe do DispositivoClasse 3

Especialidade MédicaO

Número da Regulamentação21 CFR 8

Comité consultivoOP

Resumo do dispositivo

intraocular lens is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories, LLC. It received FDA 510(k) clearance on 2026-08-17. The device is classified under product code HQL. It was reviewed by the OP advisory panel.

Perguntas frequentes

What is the intraocular lens?

intraocular lens is a medical device that received FDA 510(k) clearance on 2026-08-17. The listed applicant is Alcon Laboratories, LLC.

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 Alcon Laboratories, LLC 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.

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_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

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.