FDA 510(k)

CORGRIP* SR NG/NI Tube Retention System

N.º K: K241185 · 2024-10-25

Fecha de decisión2024-10-25

Código de productoKNT

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

CORGRIP* SR NG/NI Tube Retention System is the device name listed in this FDA 510(k) record. The listed applicant is Avanos Medical, Inc.. It received FDA 510(k) clearance on 2024-10-25 under 510(k) number K241185. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the CORGRIP* SR NG/NI Tube Retention System?

CORGRIP* SR NG/NI Tube Retention System is a medical device that received FDA 510(k) clearance on 2024-10-25. The listed applicant is Avanos Medical, Inc.. The 510(k) number is K241185.

When did CORGRIP* SR NG/NI Tube Retention System receive FDA 510(k) clearance?

CORGRIP* SR NG/NI Tube Retention System received FDA 510(k) clearance on 2024-10-25, under 510(k) number K241185.

Who is the listed applicant for CORGRIP* SR NG/NI Tube Retention System?

The FDA 510(k) record lists Avanos Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORGRIP* SR NG/NI Tube Retention System?

The FDA product code for CORGRIP* SR NG/NI Tube Retention System is KNT.

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Fuente oficial

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