FDA 510(k)

CORGRIP* SR NG/NI Tube Retention System

Número K: K241185 · 2024-10-25

Data da decisão2024-10-25

Código do produtoKNT

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do 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.

Perguntas frequentes

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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Fonte oficial

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