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FDA 510(k)

Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters

N.º K: K231015 · 2024-07-01

SolicitanteInnovative Health, LLC
Fecha de decisión2024-07-01
Código de productoNLI
Comité asesorCV
DecisiónSubstantially Equivalent

Resumen del dispositivo

Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Health, LLC. It received FDA 510(k) clearance on 2024-07-01 under 510(k) number K231015. The device is classified under product code NLI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters?

Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters is a medical device that received FDA 510(k) clearance on 2024-07-01. The listed applicant is Innovative Health, LLC. The 510(k) number is K231015.

When did Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters receive FDA 510(k) clearance?

Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters received FDA 510(k) clearance on 2024-07-01, under 510(k) number K231015.

Who is the listed applicant for Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters?

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

What is the FDA product code for Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters?

The FDA product code for Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters is NLI.

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Otros registros que enlistan a Innovative Health, LLC como solicitante

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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Ver todos los 48 dispositivos →

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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