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PMA de la FDA

Intraocular pressure lowering implant

Número de PMA: P150037 · 2020-04-09

SolicitanteAlcon Research, Ltd.
Fecha de decisión2020-04-09
Número PMAP150037
Código de productoOGO
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorOP

Resumen del dispositivo

Intraocular pressure lowering implant is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Research, Ltd.. It received FDA 510(k) clearance on 2020-04-09. The device is classified under product code OGO. It was reviewed by the OP advisory panel.

Preguntas frecuentes

What is the Intraocular pressure lowering implant?

Intraocular pressure lowering implant is a medical device that received FDA 510(k) clearance on 2020-04-09. The listed applicant is Alcon Research, Ltd..

When did Intraocular pressure lowering implant receive FDA 510(k) clearance?

The clearance date for Intraocular pressure lowering implant can be found in the official FDA records.

Who is the listed applicant for Intraocular pressure lowering implant?

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

What is the FDA product code for Intraocular pressure lowering implant?

The FDA product code for Intraocular pressure lowering implant is OGO.

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Fuente oficial

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