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PMA de la FDA

System, laser, photodynamic therapy

Número de PMA: P990021 · 2022-03-02

SolicitantePinnacle Biologics, Inc.
Fecha de decisión2022-03-02
Número PMAP990021
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 Pinnacle Biologics, Inc.. It received FDA 510(k) clearance on 2022-03-02. 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 2022-03-02. The listed applicant is Pinnacle Biologics, 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 Pinnacle Biologics, 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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