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PMA de la FDA

Device, thermal ablation, endometrial

Número de PMA: P180032 · 2026-09-15

SolicitanteChannel Medsystems, Inc.
Fecha de decisión2026-09-15
Número PMAP180032
Código de productoMNB
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorOB

Resumen del dispositivo

Device, thermal ablation, endometrial is the device name listed in this FDA 510(k) record. The listed applicant is Channel Medsystems, Inc.. It received FDA 510(k) clearance on 2026-09-15. The device is classified under product code MNB. It was reviewed by the OB advisory panel.

Preguntas frecuentes

What is the Device, thermal ablation, endometrial?

Device, thermal ablation, endometrial is a medical device that received FDA 510(k) clearance on 2026-09-15. The listed applicant is Channel Medsystems, Inc..

When did Device, thermal ablation, endometrial receive FDA 510(k) clearance?

The clearance date for Device, thermal ablation, endometrial can be found in the official FDA records.

Who is the listed applicant for Device, thermal ablation, endometrial?

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

What is the FDA product code for Device, thermal ablation, endometrial?

The FDA product code for Device, thermal ablation, endometrial is MNB.

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Fuente oficial

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