FDA PMA

Fluid, intraocular

Número do PMA: P910071 · 2025-12-22

RequerenteBausch & Lomb

Data da decisão2025-12-22

Número PMAP910071

Código do produtoLWL

Classe do DispositivoClasse 3

Especialidade MédicaO

Número da Regulamentação21 CFR 8

Comité consultivoOP

Resumo do dispositivo

Fluid, intraocular is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb. It received FDA 510(k) clearance on 2025-12-22. The device is classified under product code LWL. It was reviewed by the OP advisory panel.

Perguntas frequentes

What is the Fluid, intraocular?

Fluid, intraocular is a medical device that received FDA 510(k) clearance on 2025-12-22. The listed applicant is Bausch & Lomb.

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 Bausch & Lomb 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.

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Fonte oficial

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