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FDA 510(k)

Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller

N.º K: K251170 · 2025-09-12

SolicitanteTangent Endoscopy, LLC
Fecha de decisión2025-09-12
Código de productoFBN
Comité asesorGU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller is the device name listed in this FDA 510(k) record. The listed applicant is Tangent Endoscopy, LLC. It received FDA 510(k) clearance on 2025-09-12 under 510(k) number K251170. The device is classified under product code FBN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller?

Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller is a medical device that received FDA 510(k) clearance on 2025-09-12. The listed applicant is Tangent Endoscopy, LLC. The 510(k) number is K251170.

When did Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller receive FDA 510(k) clearance?

Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller received FDA 510(k) clearance on 2025-09-12, under 510(k) number K251170.

Who is the listed applicant for Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller?

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

What is the FDA product code for Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller?

The FDA product code for Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller is FBN.

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Fuente oficial

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