FDA PMA

Artificial iris

Número do PMA: P170039 · 2020-09-04

RequerenteHumanoptics AG

Data da decisão2020-09-04

Número PMAP170039

Código do produtoQBT

Classe do DispositivoClasse 3

Especialidade MédicaU

Comité consultivoOP

Resumo do dispositivo

Artificial iris is the device name listed in this FDA 510(k) record. The listed applicant is Humanoptics AG. It received FDA 510(k) clearance on 2020-09-04. The device is classified under product code QBT. It was reviewed by the OP advisory panel.

Perguntas frequentes

What is the Artificial iris?

Artificial iris is a medical device that received FDA 510(k) clearance on 2020-09-04. The listed applicant is Humanoptics AG.

When did Artificial iris receive FDA 510(k) clearance?

The clearance date for Artificial iris can be found in the official FDA records.

Who is the listed applicant for Artificial iris?

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

What is the FDA product code for Artificial iris?

The FDA product code for Artificial iris is QBT.

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Fonte oficial

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