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PMA de la FDA

System, laser, photodynamic therapy

Número de PMA: P990019 · 2025-05-01

SolicitanteSun Pharmaceutical Industries, Inc.
Fecha de decisión2025-05-01
Número PMAP990019
Código de productoMVF
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorSU

Resumen del dispositivo

System, laser, photodynamic therapy is the device name listed in this FDA 510(k) record. The listed applicant is Sun Pharmaceutical Industries, Inc.. It received FDA 510(k) clearance on 2025-05-01. The device is classified under product code MVF. It was reviewed by the SU advisory panel.

Preguntas frecuentes

What is the System, laser, photodynamic therapy?

System, laser, photodynamic therapy is a medical device that received FDA 510(k) clearance on 2025-05-01. The listed applicant is Sun Pharmaceutical Industries, Inc..

When did System, laser, photodynamic therapy receive FDA 510(k) clearance?

The clearance date for System, laser, photodynamic therapy can be found in the official FDA records.

Who is the listed applicant for System, laser, photodynamic therapy?

The FDA 510(k) record lists Sun Pharmaceutical Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for System, laser, photodynamic therapy?

The FDA product code for System, laser, photodynamic therapy is MVF.

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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.

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