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PMA de la FDA

Light source system, diagnostic endoscopic

Número de PMA: P050027 · 2026-07-21

SolicitanteKARL STORZ Endoscopy-America, Inc.
Fecha de decisión2026-07-21
Número PMAP050027
Código de productoOAY
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorGU

Resumen del dispositivo

Light source system, diagnostic endoscopic is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 2026-07-21. The device is classified under product code OAY. It was reviewed by the GU advisory panel.

Preguntas frecuentes

What is the Light source system, diagnostic endoscopic?

Light source system, diagnostic endoscopic is a medical device that received FDA 510(k) clearance on 2026-07-21. The listed applicant is KARL STORZ Endoscopy-America, Inc..

When did Light source system, diagnostic endoscopic receive FDA 510(k) clearance?

The clearance date for Light source system, diagnostic endoscopic can be found in the official FDA records.

Who is the listed applicant for Light source system, diagnostic endoscopic?

The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Light source system, diagnostic endoscopic?

The FDA product code for Light source system, diagnostic endoscopic is OAY.

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Fuente oficial

Ver en la base de datos de la FDA →

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