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PMA de la FDA

STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT

Número de PMA: P250011 · 2026-09-24

SolicitanteProverum, Ltd.
Fecha de decisión2026-09-24
Número PMAP250011
Código de productoMER
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorGU

Resumen del dispositivo

STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT is the device name listed in this FDA 510(k) record. The listed applicant is Proverum, Ltd.. It received FDA 510(k) clearance on 2026-09-24. The device is classified under product code MER. It was reviewed by the GU advisory panel.

Preguntas frecuentes

What is the STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT?

STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT is a medical device that received FDA 510(k) clearance on 2026-09-24. The listed applicant is Proverum, Ltd..

When did STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT receive FDA 510(k) clearance?

The clearance date for STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT can be found in the official FDA records.

Who is the listed applicant for STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT?

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

What is the FDA product code for STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT?

The FDA product code for STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT is MER.

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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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