FDA 510(k)

Endoscopio de Longitud Extendida de 7 mm

N.º K: K191930 · 2020-04-15

Fecha de decisión2020-04-15

Código de productoGCJ

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

7 mm Extended Length Endoscope is the device name listed in this FDA 510(k) record. The listed applicant is Maquet Cardiovascular, LLC. It received FDA 510(k) clearance on 2020-04-15 under 510(k) number K191930. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the 7 mm Extended Length Endoscope?

7 mm Extended Length Endoscope is a medical device that received FDA 510(k) clearance on 2020-04-15. The listed applicant is Maquet Cardiovascular, LLC. The 510(k) number is K191930.

When did 7 mm Extended Length Endoscope receive FDA 510(k) clearance?

7 mm Extended Length Endoscope received FDA 510(k) clearance on 2020-04-15, under 510(k) number K191930.

Who is the listed applicant for 7 mm Extended Length Endoscope?

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

What is the FDA product code for 7 mm Extended Length Endoscope?

The FDA product code for 7 mm Extended Length Endoscope is GCJ.

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Otros registros que enlistan a Maquet Cardiovascular, LLC como solicitante

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