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FDA 510(k)

ITrack Advance Canaloplasty Microcatheter with Advanced Delivery System

N.º K: K221872 · 2023-03-30

SolicitanteNova Eye Inc. (Business Name Nova Eye Medical)
Fecha de decisión2023-03-30
Código de productoMPA
Comité asesorGU
DecisiónSubstantially Equivalent

Resumen del dispositivo

ITrack Advance Canaloplasty Microcatheter with Advanced Delivery System is the device name listed in this FDA 510(k) record. The listed applicant is Nova Eye Inc. (Business Name Nova Eye Medical). It received FDA 510(k) clearance on 2023-03-30 under 510(k) number K221872. The device is classified under product code MPA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ITrack Advance Canaloplasty Microcatheter with Advanced Delivery System?

ITrack Advance Canaloplasty Microcatheter with Advanced Delivery System is a medical device that received FDA 510(k) clearance on 2023-03-30. The listed applicant is Nova Eye Inc. (Business Name Nova Eye Medical). The 510(k) number is K221872.

When did ITrack Advance Canaloplasty Microcatheter with Advanced Delivery System receive FDA 510(k) clearance?

ITrack Advance Canaloplasty Microcatheter with Advanced Delivery System received FDA 510(k) clearance on 2023-03-30, under 510(k) number K221872.

Who is the listed applicant for ITrack Advance Canaloplasty Microcatheter with Advanced Delivery System?

The FDA 510(k) record lists Nova Eye Inc. (Business Name Nova Eye Medical) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ITrack Advance Canaloplasty Microcatheter with Advanced Delivery System?

The FDA product code for ITrack Advance Canaloplasty Microcatheter with Advanced Delivery System is MPA.

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Dispositivos relacionados (Código: MPA)

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.

K253468Nova Eye iTrack™ 250A Canaloplasty Microcatheter (iTrack™ 250A)Nova Eye, Inc.K242184Alcon 27GA Chandelier (8065000252); Alcon 27+ DS Wide Angle Endoilluminator (8065000253); Alcon 27+ DS Endoilluminator (8065000256);Alcon Laboratories, Inc.K233653Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfield Light Pipe, 27ga (3269.M04-00)Peregrine Surgical, LLCK202670Nam illumination probe with chopperOculight , Ltd.

Fuente oficial

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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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